Canonical Allele Identifier: CA1156891756

Gene: ALDH4A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.18902073T= , CM000663.2:g.18902073T=	GRCh38
NC_000001.10:g.19228567T= , CM000663.1:g.19228567T=	GRCh37
NC_000001.9:g.19101154T=	NCBI36
NG_012283.1:g.5727A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375341.8:c.62+389A= MANE Select	ENSP00000364490.3:n.62+389A=
ENST00000290597.9:c.62+389A=	ENSP00000290597.5:n.62+389A=
ENST00000375341.7:c.62+389A=	ENSP00000364490.3:n.62+389A=
ENST00000432718.1:c.62+389A=	ENSP00000393209.1:n.62+389A=
ENST00000494072.3:c.911+6466A=
ENST00000538839.5:c.62+389A=	ENSP00000446071.1:n.62+389A=
NM_003748.3:c.62+389A=	NP_003739.2:n.62+389A=
NM_170726.2:c.62+389A=	NP_733844.1:n.62+389A=
XM_011542352.1:c.62+389A=	XP_011540654.1:n.62+389A=
XM_011542353.1:c.62+389A=	XP_011540655.1:n.62+389A=
XR_946786.1:n.119+389A=
NM_001319218.1:c.62+389A=	NP_001306147.1:n.62+389A=
XR_001737510.1:n.119+389A=
NM_003748.4:c.62+389A= MANE Select	NP_003739.2:n.62+389A=
NM_170726.3:c.62+389A=	NP_733844.1:n.62+389A=
NM_001319218.2:c.62+389A=	NP_001306147.1:n.62+389A=