Canonical Allele Identifier: CA363419177

Gene: HSPA1A HSPA1L

Linked Data

• MyVariant Identifiers: chr6:g.31817241_31817243del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31817242_31817244del , CM000668.2:g.31817242_31817244del	GRCh38
NC_000006.11:g.31785019_31785021del , CM000668.1:g.31785019_31785021del	GRCh37
NC_000006.10:g.31892998_31893000del	NCBI36
NG_011855.1:g.2816_2818del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375651.7:c.1486_1488del (HSPA1A) MANE Select	ENSP00000364802.5:p.Gly496del
ENST00000375651.6:c.1486_1488del (HSPA1A)	ENSP00000364802.5:p.Gly496del
ENST00000608703.1:c.991_993del (HSPA1A)	ENSP00000477378.1:p.Gly331del
NM_005345.5:c.1486_1488del (HSPA1A)	NP_005336.3:p.Gly496del
XM_005249073.2:c.-14+3770_-14+3772del (HSPA1L)	XP_005249130.1:n.-14+3770_-14+3772del
XM_011514566.1:c.-14+3770_-14+3772del (HSPA1L)	XP_011512868.1:n.-14+3770_-14+3772del
NM_005345.6:c.1486_1488del (HSPA1A) MANE Select	NP_005336.3:p.Gly496del