Canonical Allele Identifier: CA2245709670
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222791C= , CM000679.2:g.7222791C= GRCh38
NC_000017.10:g.7126110C= , CM000679.1:g.7126110C= GRCh37
NC_000017.9:g.7066834C= NCBI36
NG_007975.1:g.7958C=
NG_008391.2:g.2260G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1003C= MANE Select ENSP00000349297.5:p.His335=
ENST00000322910.9:c.*958C= ENSP00000325395.5:n.*958C=
ENST00000350303.9:c.937C= ENSP00000344152.5:p.His313=
ENST00000356839.9:c.1003C= ENSP00000349297.5:p.His335=
ENST00000543245.6:c.1072C= ENSP00000438689.2:p.His358=
ENST00000578824.5:n.152C=
ENST00000581378.5:c.721C=
ENST00000582379.1:n.387C=
ENST00000583858.5:c.32C=
NM_000018.3:c.1003C= NP_000009.1:p.His335=
NM_001033859.2:c.937C= NP_001029031.1:p.His313=
NM_001270447.1:c.1072C= NP_001257376.1:p.His358=
NM_001270448.1:c.775C= NP_001257377.1:p.His259=
XM_006721516.2:c.1003C= XP_006721579.2:p.His335=
XM_011523829.1:c.1003C= XP_011522131.1:p.His335=
XM_011523830.1:c.1003C= XP_011522132.1:p.His335=
XR_934021.1:n.1110C=
XR_934022.1:n.1110C=
XR_934023.1:n.1110C=
XM_006721516.3:c.1003C= XP_006721579.2:p.His335=
XM_011523829.2:c.1003C= XP_011522131.1:p.His335=
XM_011523830.2:c.1003C= XP_011522132.1:p.His335=
XM_024450741.1:c.1003C= XP_024306509.1:p.His335=
XR_934021.2:n.1062C=
XR_934022.2:n.1062C=
XR_934023.2:n.1062C=
NM_000018.4:c.1003C= MANE Select NP_000009.1:p.His335=
NM_001033859.3:c.937C= NP_001029031.1:p.His313=
NM_001270447.2:c.1072C= NP_001257376.1:p.His358=
NM_001270448.2:c.775C= NP_001257377.1:p.His259=