Canonical Allele Identifier: CA275603458
Gene: ALDH1A3 HGNC NCBI

Linked Data

dbSNP Id: rs75726102
gnomAD v2: 15-101428086-C-T
gnomAD v3: 15-100887881-C-T
gnomAD v4: 15-100887881-C-T
MyVariant Identifiers: chr15:g.101428086C>T (hg19) chr15:g.101428086_101428095delinsTTAGACTGAA (hg19) chr15:g.100887881C>T (hg38) chr15:g.100887881_100887890delinsTTAGACTGAA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.100887881C>T , CM000677.2:g.100887881C>T GRCh38
NC_000015.9:g.101428086C>T , CM000677.1:g.101428086C>T GRCh37
NC_000015.8:g.99245609C>T NCBI36
NG_012254.1:g.13078C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000329841.10:c.345+169C>T MANE Select ENSP00000332256.5:n.345+169C>T
ENST00000329841.9:c.345+169C>T ENSP00000332256.5:n.345+169C>T
ENST00000346623.6:c.345+169C>T ENSP00000343294.6:n.345+169C>T
ENST00000558033.5:c.345+169C>T ENSP00000454107.1:n.345+169C>T
ENST00000560555.1:n.405+169C>T
ENST00000561338.5:c.261+169C>T ENSP00000452789.1:n.261+169C>T
NM_000693.3:c.345+169C>T NP_000684.2:n.345+169C>T
NM_001293815.1:c.345+169C>T NP_001280744.1:n.345+169C>T
NM_000693.4:c.345+169C>T MANE Select NP_000684.2:n.345+169C>T
NM_001293815.2:c.345+169C>T NP_001280744.1:n.345+169C>T
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