Canonical Allele Identifier: CA1616509935
Gene: ALDH5A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24503103_24503104delinsCT , CM000668.2:g.24503103_24503104delinsCT GRCh38
NC_000006.11:g.24503331_24503332delinsCT , CM000668.1:g.24503331_24503332delinsCT GRCh37
NC_000006.10:g.24611310_24611311delinsCT NCBI36
NG_008161.1:g.13135_13136delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000357578.8:c.439-160_439-159delinsCT MANE Select ENSP00000350191.3:n.439-160_439-159delinsCT
ENST00000672352.1:c.202-160_202-159delinsCT ENSP00000500876.1:n.202-160_202-159delinsCT
ENST00000672557.1:c.357-160_357-159delinsCT
ENST00000672652.1:c.360-160_360-159delinsCT
ENST00000675422.1:n.1199-160_1199-159delinsCT
ENST00000348925.2:c.439-160_439-159delinsCT ENSP00000314649.3:n.439-160_439-159delinsCT
ENST00000357578.7:c.439-160_439-159delinsCT ENSP00000350191.3:n.439-160_439-159delinsCT
ENST00000491546.5:c.355-160_355-159delinsCT ENSP00000417687.1:n.355-160_355-159delinsCT
NM_001080.3:c.439-160_439-159delinsCT MANE Select NP_001071.1:n.439-160_439-159delinsCT
NM_170740.1:c.439-160_439-159delinsCT NP_733936.1:n.439-160_439-159delinsCT
NM_001368954.1:c.439-160_439-159delinsCT NP_001355883.1:n.439-160_439-159delinsCT