Canonical Allele Identifier: CA2643744333
Gene: ALDH4A1 HGNC NCBI

Linked Data

gnomAD v4: 1-18902413-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.18902413C>G , CM000663.2:g.18902413C>G GRCh38
NC_000001.10:g.19228907C>G , CM000663.1:g.19228907C>G GRCh37
NC_000001.9:g.19101494C>G NCBI36
NG_012283.1:g.5387G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000375341.8:c.62+49G>C MANE Select ENSP00000364490.3:n.62+49G>C
ENST00000290597.9:c.62+49G>C ENSP00000290597.5:n.62+49G>C
ENST00000375341.7:c.62+49G>C ENSP00000364490.3:n.62+49G>C
ENST00000432718.1:c.62+49G>C ENSP00000393209.1:n.62+49G>C
ENST00000494072.3:c.911+6126G>C
ENST00000538839.5:c.62+49G>C ENSP00000446071.1:n.62+49G>C
NM_003748.3:c.62+49G>C NP_003739.2:n.62+49G>C
NM_170726.2:c.62+49G>C NP_733844.1:n.62+49G>C
XM_011542352.1:c.62+49G>C XP_011540654.1:n.62+49G>C
XM_011542353.1:c.62+49G>C XP_011540655.1:n.62+49G>C
XR_946786.1:n.119+49G>C
NM_001319218.1:c.62+49G>C NP_001306147.1:n.62+49G>C
XR_001737510.1:n.119+49G>C
NM_003748.4:c.62+49G>C MANE Select NP_003739.2:n.62+49G>C
NM_170726.3:c.62+49G>C NP_733844.1:n.62+49G>C
NM_001319218.2:c.62+49G>C NP_001306147.1:n.62+49G>C