Canonical Allele Identifier: CA397724655
Gene: ACADVL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7223695C>A , CM000679.2:g.7223695C>A GRCh38
NC_000017.10:g.7127014C>A , CM000679.1:g.7127014C>A GRCh37
NC_000017.9:g.7067738C>A NCBI36
NG_007975.1:g.8862C>A
NG_008391.2:g.1356G>T
NG_033038.1:g.15850G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1234C>A MANE Select ENSP00000349297.5:p.Gln412Lys
ENST00000322910.9:c.*1189C>A ENSP00000325395.5:n.*1189C>A
ENST00000350303.9:c.1168C>A ENSP00000344152.5:p.Gln390Lys
ENST00000356839.9:c.1234C>A ENSP00000349297.5:p.Gln412Lys
ENST00000542255.6:c.92C>A
ENST00000543245.6:c.1303C>A ENSP00000438689.2:p.Gln435Lys
ENST00000578579.2:n.405C>A
ENST00000578711.1:n.191C>A
ENST00000578824.5:n.650C>A
ENST00000579425.5:n.258C>A
ENST00000579546.1:c.71C>A
ENST00000583850.5:n.9C>A
ENST00000583858.5:c.263C>A
ENST00000585203.6:n.442C>A
NM_000018.3:c.1234C>A NP_000009.1:p.Gln412Lys
NM_001033859.2:c.1168C>A NP_001029031.1:p.Gln390Lys
NM_001270447.1:c.1303C>A NP_001257376.1:p.Gln435Lys
NM_001270448.1:c.1006C>A NP_001257377.1:p.Gln336Lys
XM_006721516.2:c.1234C>A XP_006721579.2:p.Gln412Lys
XM_011523829.1:c.1234C>A XP_011522131.1:p.Gln412Lys
XM_011523830.1:c.1234C>A XP_011522132.1:p.Gln412Lys
XR_934021.1:n.1341C>A
XR_934022.1:n.1341C>A
XR_934023.1:n.1341C>A
XM_006721516.3:c.1234C>A XP_006721579.2:p.Gln412Lys
XM_011523829.2:c.1234C>A XP_011522131.1:p.Gln412Lys
XM_011523830.2:c.1234C>A XP_011522132.1:p.Gln412Lys
XM_024450741.1:c.1234C>A XP_024306509.1:p.Gln412Lys
XR_934021.2:n.1293C>A
XR_934022.2:n.1293C>A
XR_934023.2:n.1293C>A
NM_000018.4:c.1234C>A MANE Select NP_000009.1:p.Gln412Lys
NM_001033859.3:c.1168C>A NP_001029031.1:p.Gln390Lys
NM_001270447.2:c.1303C>A NP_001257376.1:p.Gln435Lys
NM_001270448.2:c.1006C>A NP_001257377.1:p.Gln336Lys