Canonical Allele Identifier: CA397725592
Gene: ACADVL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224535A>T , CM000679.2:g.7224535A>T GRCh38
NC_000017.10:g.7127854A>T , CM000679.1:g.7127854A>T GRCh37
NC_000017.9:g.7068578A>T NCBI36
NG_007975.1:g.9702A>T
NG_008391.2:g.516T>A
NG_033038.1:g.15010T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1661A>T MANE Select ENSP00000349297.5:p.His554Leu
ENST00000322910.9:c.*1616A>T ENSP00000325395.5:n.*1616A>T
ENST00000350303.9:c.1595A>T ENSP00000344152.5:p.His532Leu
ENST00000356839.9:c.1661A>T ENSP00000349297.5:p.His554Leu
ENST00000542255.6:c.519A>T
ENST00000543245.6:c.1730A>T ENSP00000438689.2:p.His577Leu
ENST00000578319.5:n.242A>T
ENST00000578711.1:n.1031A>T
ENST00000578809.5:n.233A>T
ENST00000579391.1:n.265A>T
ENST00000579425.5:n.777A>T
ENST00000579546.1:c.396A>T
ENST00000582450.1:n.169A>T
ENST00000583074.5:n.282A>T
ENST00000583848.5:c.47A>T ENSP00000466487.1:p.His16Leu
ENST00000583850.5:n.432A>T
ENST00000583858.5:c.592A>T
ENST00000585203.6:n.852A>T
NM_000018.3:c.1661A>T NP_000009.1:p.His554Leu
NM_001033859.2:c.1595A>T NP_001029031.1:p.His532Leu
NM_001270447.1:c.1730A>T NP_001257376.1:p.His577Leu
NM_001270448.1:c.1433A>T NP_001257377.1:p.His478Leu
XM_006721516.2:c.1661A>T XP_006721579.2:p.His554Leu
XM_011523829.1:c.1559A>T XP_011522131.1:p.His520Leu
XM_011523830.1:c.1559A>T XP_011522132.1:p.His520Leu
XR_934021.1:n.1764A>T
XR_934022.1:n.1670A>T
XR_934023.1:n.1670A>T
XM_006721516.3:c.1661A>T XP_006721579.2:p.His554Leu
XM_011523829.2:c.1559A>T XP_011522131.1:p.His520Leu
XM_011523830.2:c.1559A>T XP_011522132.1:p.His520Leu
XM_024450741.1:c.1649A>T XP_024306509.1:p.His550Leu
XR_934021.2:n.1716A>T
XR_934022.2:n.1622A>T
XR_934023.2:n.1622A>T
NM_000018.4:c.1661A>T MANE Select NP_000009.1:p.His554Leu
NM_001033859.3:c.1595A>T NP_001029031.1:p.His532Leu
NM_001270447.2:c.1730A>T NP_001257376.1:p.His577Leu
NM_001270448.2:c.1433A>T NP_001257377.1:p.His478Leu