Canonical Allele Identifier: CA492418108
Gene: ALDH1A3 HGNC NCBI
ALDH1A3-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1295413746
gnomAD v4: 15-100915041-G-A
MyVariant Identifiers: chr15:g.101455246G>A (hg19) chr15:g.100915041G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.100915041G>A , CM000677.2:g.100915041G>A GRCh38
NC_000015.9:g.101455246G>A , CM000677.1:g.101455246G>A GRCh37
NC_000015.8:g.99272769G>A NCBI36
NG_012254.1:g.40238G>A
NG_052791.1:g.1025G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000329841.10:c.*268G>A (ALDH1A3) MANE Select ENSP00000332256.5:n.*268G>A
ENST00000329841.9:c.*268G>A (ALDH1A3) ENSP00000332256.5:n.*268G>A
ENST00000346623.6:c.*268G>A (ALDH1A3) ENSP00000343294.6:n.*268G>A
NM_000693.3:c.*268G>A (ALDH1A3) NP_000684.2:n.*268G>A
NM_001293815.1:c.*268G>A (ALDH1A3) NP_001280744.1:n.*268G>A
NR_135827.1:n.480+3763C>T (ALDH1A3-AS1)
NR_135828.1:n.1420C>T (ALDH1A3-AS1)
NR_135831.1:n.2336C>T (ALDH1A3-AS1)
NM_000693.4:c.*268G>A (ALDH1A3) MANE Select NP_000684.2:n.*268G>A
NM_001293815.2:c.*268G>A (ALDH1A3) NP_001280744.1:n.*268G>A
Search 100 bp 5'
Search 100 bp 3'