Canonical Allele Identifier: CA275603105
Gene: ALDH1A3 HGNC NCBI

Linked Data

dbSNP Id: rs28557216
gnomAD v2: 15-101427645-G-C
gnomAD v3: 15-100887440-G-C
gnomAD v4: 15-100887440-G-C
MyVariant Identifiers: chr15:g.101427645G>C (hg19) chr15:g.101427645_101427675delinsCTCAAAAGATGACACCCAAACTGCAGTCACC (hg19) chr15:g.100887440G>C (hg38) chr15:g.100887440_100887470delinsCTCAAAAGATGACACCCAAACTGCAGTCACC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.100887440G>C , CM000677.2:g.100887440G>C GRCh38
NC_000015.9:g.101427645G>C , CM000677.1:g.101427645G>C GRCh37
NC_000015.8:g.99245168G>C NCBI36
NG_012254.1:g.12637G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000329841.10:c.205-132G>C MANE Select ENSP00000332256.5:n.205-132G>C
ENST00000329841.9:c.205-132G>C ENSP00000332256.5:n.205-132G>C
ENST00000346623.6:c.205-132G>C ENSP00000343294.6:n.205-132G>C
ENST00000558033.5:c.205-132G>C ENSP00000454107.1:n.205-132G>C
ENST00000560555.1:n.265-132G>C
ENST00000561338.5:c.121-132G>C ENSP00000452789.1:n.121-132G>C
NM_000693.3:c.205-132G>C NP_000684.2:n.205-132G>C
NM_001293815.1:c.205-132G>C NP_001280744.1:n.205-132G>C
NM_000693.4:c.205-132G>C MANE Select NP_000684.2:n.205-132G>C
NM_001293815.2:c.205-132G>C NP_001280744.1:n.205-132G>C
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