Canonical Allele Identifier: CA2200270191

Gene: ALDH1A3 ALDH1A3-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100914589_100914590delinsCT , CM000677.2:g.100914589_100914590delinsCT	GRCh38
NC_000015.9:g.101454794_101454795delinsCT , CM000677.1:g.101454794_101454795delinsCT	GRCh37
NC_000015.8:g.99272317_99272318delinsCT	NCBI36
NG_012254.1:g.39786_39787delinsCT
NG_052791.1:g.573_574delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329841.10:c.1467-112_1467-111delinsCT (ALDH1A3) MANE Select	ENSP00000332256.5:n.1467-112_1467-111delinsCT
ENST00000329841.9:c.1467-112_1467-111delinsCT (ALDH1A3)	ENSP00000332256.5:n.1467-112_1467-111delinsCT
ENST00000346623.6:c.1146-112_1146-111delinsCT (ALDH1A3)	ENSP00000343294.6:n.1146-112_1146-111delinsCT
NM_000693.3:c.1467-112_1467-111delinsCT (ALDH1A3)	NP_000684.2:n.1467-112_1467-111delinsCT
NM_001293815.1:c.1146-112_1146-111delinsCT (ALDH1A3)	NP_001280744.1:n.1146-112_1146-111delinsCT
NR_135827.1:n.480+4214_480+4215delinsAG (ALDH1A3-AS1)
NR_135828.1:n.1871_1872delinsAG (ALDH1A3-AS1)
NR_135831.1:n.2787_2788delinsAG (ALDH1A3-AS1)
NM_000693.4:c.1467-112_1467-111delinsCT (ALDH1A3) MANE Select	NP_000684.2:n.1467-112_1467-111delinsCT
NM_001293815.2:c.1146-112_1146-111delinsCT (ALDH1A3)	NP_001280744.1:n.1146-112_1146-111delinsCT