Canonical Allele Identifier: CA1619307635

Gene: HSPA1A HSPA1L

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31817258_31817261delinsTCAC , CM000668.2:g.31817258_31817261delinsTCAC	GRCh38
NC_000006.11:g.31785035_31785038delinsTCAC , CM000668.1:g.31785035_31785038delinsTCAC	GRCh37
NC_000006.10:g.31893014_31893017delinsTCAC	NCBI36
NG_011855.1:g.2798_2801delinsGTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375651.7:c.1502_1505delinsTCAC (HSPA1A) MANE Select	ENSP00000364802.5:p.Ile501=
ENST00000375651.6:c.1502_1505delinsTCAC (HSPA1A)	ENSP00000364802.5:p.Ile501=
ENST00000608703.1:c.1007_1010delinsTCAC (HSPA1A)	ENSP00000477378.1:p.Ile336=
NM_005345.5:c.1502_1505delinsTCAC (HSPA1A)	NP_005336.3:p.Ile501=
XM_005249073.2:c.-14+3752_-14+3755delinsGTGA (HSPA1L)	XP_005249130.1:n.-14+3752_-14+3755delinsGTGA
XM_011514566.1:c.-14+3752_-14+3755delinsGTGA (HSPA1L)	XP_011512868.1:n.-14+3752_-14+3755delinsGTGA
NM_005345.6:c.1502_1505delinsTCAC (HSPA1A) MANE Select	NP_005336.3:p.Ile501=