Canonical Allele Identifier: CA620120910

Gene: ALDH1A3

Linked Data

• dbSNP Id: rs1567168092
• gnomAD v2: 15-101427675-CTCAAAAGATGACACCCAAACTTCAGTCACGTCAAAAGATGACACCCAAACTGCAGTCACG-C
• gnomAD v3: 15-100887470-CTCAAAAGATGACACCCAAACTTCAGTCACGTCAAAAGATGACACCCAAACTGCAGTCACG-C
• gnomAD v4: 15-100887470-CTCAAAAGATGACACCCAAACTTCAGTCACGTCAAAAGATGACACCCAAACTGCAGTCACG-C
• MyVariant Identifiers: chr15:g.101427676_101427735del (hg19) ; chr15:g.100887471_100887530del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100887484_100887543del , CM000677.2:g.100887484_100887543del	GRCh38
NC_000015.9:g.101427689_101427748del , CM000677.1:g.101427689_101427748del	GRCh37
NC_000015.8:g.99245212_99245271del	NCBI36
NG_012254.1:g.12681_12740del

Transcript Alleles

HGVS	Amino-acid change
ENST00000329841.10:c.205-88_205-29del MANE Select	ENSP00000332256.5:n.205-88_205-29del
ENST00000329841.9:c.205-88_205-29del	ENSP00000332256.5:n.205-88_205-29del
ENST00000346623.6:c.205-88_205-29del	ENSP00000343294.6:n.205-88_205-29del
ENST00000558033.5:c.205-88_205-29del	ENSP00000454107.1:n.205-88_205-29del
ENST00000560555.1:n.265-88_265-29del
ENST00000561338.5:c.121-88_121-29del	ENSP00000452789.1:n.121-88_121-29del
NM_000693.3:c.205-88_205-29del	NP_000684.2:n.205-88_205-29del
NM_001293815.1:c.205-88_205-29del	NP_001280744.1:n.205-88_205-29del
NM_000693.4:c.205-88_205-29del MANE Select	NP_000684.2:n.205-88_205-29del
NM_001293815.2:c.205-88_205-29del	NP_001280744.1:n.205-88_205-29del