Canonical Allele Identifier: CA1156891901

Gene: ALDH4A1

Linked Data

• dbSNP Id: rs1935829101
• gnomAD v4: 1-18902371-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.18902371A>G , CM000663.2:g.18902371A>G	GRCh38
NC_000001.10:g.19228865A>G , CM000663.1:g.19228865A>G	GRCh37
NC_000001.9:g.19101452A>G	NCBI36
NG_012283.1:g.5429T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375341.8:c.62+91T>C MANE Select	ENSP00000364490.3:n.62+91T>C
ENST00000290597.9:c.62+91T>C	ENSP00000290597.5:n.62+91T>C
ENST00000375341.7:c.62+91T>C	ENSP00000364490.3:n.62+91T>C
ENST00000432718.1:c.62+91T>C	ENSP00000393209.1:n.62+91T>C
ENST00000494072.3:c.911+6168T>C
ENST00000538839.5:c.62+91T>C	ENSP00000446071.1:n.62+91T>C
NM_003748.3:c.62+91T>C	NP_003739.2:n.62+91T>C
NM_170726.2:c.62+91T>C	NP_733844.1:n.62+91T>C
XM_011542352.1:c.62+91T>C	XP_011540654.1:n.62+91T>C
XM_011542353.1:c.62+91T>C	XP_011540655.1:n.62+91T>C
XR_946786.1:n.119+91T>C
NM_001319218.1:c.62+91T>C	NP_001306147.1:n.62+91T>C
XR_001737510.1:n.119+91T>C
NM_003748.4:c.62+91T>C MANE Select	NP_003739.2:n.62+91T>C
NM_170726.3:c.62+91T>C	NP_733844.1:n.62+91T>C
NM_001319218.2:c.62+91T>C	NP_001306147.1:n.62+91T>C