Canonical Allele Identifier: CA624860777
Gene: ACADVL HGNC NCBI

Linked Data

dbSNP Id: rs1189814899

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224560_7224561insTACG , CM000679.2:g.7224560_7224561insTACG GRCh38
NC_000017.10:g.7127879_7127880insTACG , CM000679.1:g.7127879_7127880insTACG GRCh37
NC_000017.9:g.7068603_7068604insTACG NCBI36
NG_007975.1:g.9727_9728insTACG
NG_008391.2:g.490_491insCGTA
NG_033038.1:g.14984_14985insCGTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1678+8_1678+9insTACG MANE Select ENSP00000349297.5:n.1678+8_1678+9insTACG
ENST00000322910.9:c.*1633+8_*1633+9insTACG ENSP00000325395.5:n.*1633+8_*1633+9insTACG
ENST00000350303.9:c.1612+8_1612+9insTACG ENSP00000344152.5:n.1612+8_1612+9insTACG
ENST00000356839.9:c.1678+8_1678+9insTACG ENSP00000349297.5:n.1678+8_1678+9insTACG
ENST00000542255.6:c.536+8_536+9insTACG
ENST00000543245.6:c.1747+8_1747+9insTACG ENSP00000438689.2:n.1747+8_1747+9insTACG
ENST00000578319.5:n.259+8_259+9insTACG
ENST00000578711.1:n.1056_1057insTACG
ENST00000578809.5:n.250+8_250+9insTACG
ENST00000579391.1:n.290_291insTACG
ENST00000579425.5:n.794+8_794+9insTACG
ENST00000579546.1:c.413+8_413+9insTACG
ENST00000582450.1:n.194_195insTACG
ENST00000583074.5:n.299+8_299+9insTACG
ENST00000583848.5:c.64+8_64+9insTACG ENSP00000466487.1:n.64+8_64+9insTACG
ENST00000583850.5:n.449+8_449+9insTACG
ENST00000583858.5:c.609+8_609+9insTACG
ENST00000585203.6:n.869+8_869+9insTACG
NM_000018.3:c.1678+8_1678+9insTACG NP_000009.1:n.1678+8_1678+9insTACG
NM_001033859.2:c.1612+8_1612+9insTACG NP_001029031.1:n.1612+8_1612+9insTACG
NM_001270447.1:c.1747+8_1747+9insTACG NP_001257376.1:n.1747+8_1747+9insTACG
NM_001270448.1:c.1450+8_1450+9insTACG NP_001257377.1:n.1450+8_1450+9insTACG
XM_006721516.2:c.1678+8_1678+9insTACG XP_006721579.2:n.1678+8_1678+9insTACG
XM_011523829.1:c.1576+8_1576+9insTACG XP_011522131.1:n.1576+8_1576+9insTACG
XM_011523830.1:c.1576+8_1576+9insTACG XP_011522132.1:n.1576+8_1576+9insTACG
XR_934021.1:n.1781+8_1781+9insTACG
XR_934022.1:n.1687+8_1687+9insTACG
XR_934023.1:n.1687+8_1687+9insTACG
XM_006721516.3:c.1678+8_1678+9insTACG XP_006721579.2:n.1678+8_1678+9insTACG
XM_011523829.2:c.1576+8_1576+9insTACG XP_011522131.1:n.1576+8_1576+9insTACG
XM_011523830.2:c.1576+8_1576+9insTACG XP_011522132.1:n.1576+8_1576+9insTACG
XM_024450741.1:c.1666+8_1666+9insTACG XP_024306509.1:n.1666+8_1666+9insTACG
XR_934021.2:n.1733+8_1733+9insTACG
XR_934022.2:n.1639+8_1639+9insTACG
XR_934023.2:n.1639+8_1639+9insTACG
NM_000018.4:c.1678+8_1678+9insTACG MANE Select NP_000009.1:n.1678+8_1678+9insTACG
NM_001033859.3:c.1612+8_1612+9insTACG NP_001029031.1:n.1612+8_1612+9insTACG
NM_001270447.2:c.1747+8_1747+9insTACG NP_001257376.1:n.1747+8_1747+9insTACG
NM_001270448.2:c.1450+8_1450+9insTACG NP_001257377.1:n.1450+8_1450+9insTACG