Canonical Allele Identifier: CA2200270216

Gene: ALDH1A3 ALDH1A3-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100914663_100914664delinsGT , CM000677.2:g.100914663_100914664delinsGT	GRCh38
NC_000015.9:g.101454868_101454869delinsGT , CM000677.1:g.101454868_101454869delinsGT	GRCh37
NC_000015.8:g.99272391_99272392delinsGT	NCBI36
NG_012254.1:g.39860_39861delinsGT
NG_052791.1:g.647_648delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329841.10:c.1467-38_1467-37delinsGT (ALDH1A3) MANE Select	ENSP00000332256.5:n.1467-38_1467-37delinsGT
ENST00000329841.9:c.1467-38_1467-37delinsGT (ALDH1A3)	ENSP00000332256.5:n.1467-38_1467-37delinsGT
ENST00000346623.6:c.1146-38_1146-37delinsGT (ALDH1A3)	ENSP00000343294.6:n.1146-38_1146-37delinsGT
NM_000693.3:c.1467-38_1467-37delinsGT (ALDH1A3)	NP_000684.2:n.1467-38_1467-37delinsGT
NM_001293815.1:c.1146-38_1146-37delinsGT (ALDH1A3)	NP_001280744.1:n.1146-38_1146-37delinsGT
NR_135827.1:n.480+4140_480+4141delinsAC (ALDH1A3-AS1)
NR_135828.1:n.1797_1798delinsAC (ALDH1A3-AS1)
NR_135831.1:n.2713_2714delinsAC (ALDH1A3-AS1)
NM_000693.4:c.1467-38_1467-37delinsGT (ALDH1A3) MANE Select	NP_000684.2:n.1467-38_1467-37delinsGT
NM_001293815.2:c.1146-38_1146-37delinsGT (ALDH1A3)	NP_001280744.1:n.1146-38_1146-37delinsGT