Canonical Allele Identifier: CA275590413

Gene: ALDH1A3 ALDH1A3-AS1

Linked Data

• dbSNP Id: rs927738589
• gnomAD v3: 15-100914926-C-T
• gnomAD v4: 15-100914926-C-T
• MyVariant Identifiers: chr15:g.101455131C>T (hg19) ; chr15:g.100914926C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100914926C>T , CM000677.2:g.100914926C>T	GRCh38
NC_000015.9:g.101455131C>T , CM000677.1:g.101455131C>T	GRCh37
NC_000015.8:g.99272654C>T	NCBI36
NG_012254.1:g.40123C>T
NG_052791.1:g.910C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329841.10:c.*153C>T (ALDH1A3) MANE Select	ENSP00000332256.5:n.*153C>T
ENST00000329841.9:c.*153C>T (ALDH1A3)	ENSP00000332256.5:n.*153C>T
ENST00000346623.6:c.*153C>T (ALDH1A3)	ENSP00000343294.6:n.*153C>T
NM_000693.3:c.*153C>T (ALDH1A3)	NP_000684.2:n.*153C>T
NM_001293815.1:c.*153C>T (ALDH1A3)	NP_001280744.1:n.*153C>T
NR_135827.1:n.480+3878G>A (ALDH1A3-AS1)
NR_135828.1:n.1535G>A (ALDH1A3-AS1)
NR_135831.1:n.2451G>A (ALDH1A3-AS1)
NM_000693.4:c.*153C>T (ALDH1A3) MANE Select	NP_000684.2:n.*153C>T
NM_001293815.2:c.*153C>T (ALDH1A3)	NP_001280744.1:n.*153C>T