Canonical Allele Identifier: CA710623928

Gene: ALDH1A3 ALDH1A3-AS1

Linked Data

• dbSNP Id: rs1406140664
• MyVariant Identifiers: chr15:g.101454987_101455000del (hg19) ; chr15:g.100914782_100914795del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100914783_100914796del , CM000677.2:g.100914783_100914796del	GRCh38
NC_000015.9:g.101454988_101455001del , CM000677.1:g.101454988_101455001del	GRCh37
NC_000015.8:g.99272511_99272524del	NCBI36
NG_012254.1:g.39980_39993del
NG_052791.1:g.767_780del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329841.10:c.*10_*23del (ALDH1A3) MANE Select	ENSP00000332256.5:n.*10_*23del
ENST00000329841.9:c.*10_*23del (ALDH1A3)	ENSP00000332256.5:n.*10_*23del
ENST00000346623.6:c.*10_*23del (ALDH1A3)	ENSP00000343294.6:n.*10_*23del
NM_000693.3:c.*10_*23del (ALDH1A3)	NP_000684.2:n.*10_*23del
NM_001293815.1:c.*10_*23del (ALDH1A3)	NP_001280744.1:n.*10_*23del
NR_135827.1:n.480+4009_480+4022del (ALDH1A3-AS1)
NR_135828.1:n.1666_1679del (ALDH1A3-AS1)
NR_135831.1:n.2582_2595del (ALDH1A3-AS1)
NM_000693.4:c.*10_*23del (ALDH1A3) MANE Select	NP_000684.2:n.*10_*23del
NM_001293815.2:c.*10_*23del (ALDH1A3)	NP_001280744.1:n.*10_*23del