Canonical Allele Identifier: CA2678045994

Gene: HSPA1A HSPA1L

Linked Data

• gnomAD v4: 6-31817232-CAAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31817234_31817236del , CM000668.2:g.31817234_31817236del	GRCh38
NC_000006.11:g.31785011_31785013del , CM000668.1:g.31785011_31785013del	GRCh37
NC_000006.10:g.31892990_31892992del	NCBI36
NG_011855.1:g.2824_2826del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375651.7:c.1478_1480del (HSPA1A) MANE Select	ENSP00000364802.5:p.Lys493del
ENST00000375651.6:c.1478_1480del (HSPA1A)	ENSP00000364802.5:p.Lys493del
ENST00000608703.1:c.983_985del (HSPA1A)	ENSP00000477378.1:p.Lys328del
NM_005345.5:c.1478_1480del (HSPA1A)	NP_005336.3:p.Lys493del
XM_005249073.2:c.-14+3778_-14+3780del (HSPA1L)	XP_005249130.1:n.-14+3778_-14+3780del
XM_011514566.1:c.-14+3778_-14+3780del (HSPA1L)	XP_011512868.1:n.-14+3778_-14+3780del
NM_005345.6:c.1478_1480del (HSPA1A) MANE Select	NP_005336.3:p.Lys493del