Canonical Allele Identifier: CA1619307625

Gene: HSPA1A HSPA1L

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31817239_31817242delinsACCG , CM000668.2:g.31817239_31817242delinsACCG	GRCh38
NC_000006.11:g.31785016_31785019delinsACCG , CM000668.1:g.31785016_31785019delinsACCG	GRCh37
NC_000006.10:g.31892995_31892998delinsACCG	NCBI36
NG_011855.1:g.2817_2820delinsCGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375651.7:c.1483_1486delinsACCG (HSPA1A) MANE Select	ENSP00000364802.5:p.Thr495=
ENST00000375651.6:c.1483_1486delinsACCG (HSPA1A)	ENSP00000364802.5:p.Thr495=
ENST00000608703.1:c.988_991delinsACCG (HSPA1A)	ENSP00000477378.1:p.Thr330=
NM_005345.5:c.1483_1486delinsACCG (HSPA1A)	NP_005336.3:p.Thr495=
XM_005249073.2:c.-14+3771_-14+3774delinsCGGT (HSPA1L)	XP_005249130.1:n.-14+3771_-14+3774delinsCGGT
XM_011514566.1:c.-14+3771_-14+3774delinsCGGT (HSPA1L)	XP_011512868.1:n.-14+3771_-14+3774delinsCGGT
NM_005345.6:c.1483_1486delinsACCG (HSPA1A) MANE Select	NP_005336.3:p.Thr495=