Canonical Allele Identifier: CA823903725

Gene: HSPA1A HSPA1L

Linked Data

• dbSNP Id: rs1458420597
• gnomAD v4: 6-31817290-AAGG-A
• MyVariant Identifiers: chr6:g.31785068_31785070del (hg19) ; chr6:g.31817291_31817293del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31817296_31817298del , CM000668.2:g.31817296_31817298del	GRCh38
NC_000006.11:g.31785073_31785075del , CM000668.1:g.31785073_31785075del	GRCh37
NC_000006.10:g.31893052_31893054del	NCBI36
NG_011855.1:g.2766_2768del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375651.7:c.1540_1542del (HSPA1A) MANE Select	ENSP00000364802.5:p.Glu514del
ENST00000375651.6:c.1540_1542del (HSPA1A)	ENSP00000364802.5:p.Glu514del
ENST00000608703.1:c.1045_1047del (HSPA1A)	ENSP00000477378.1:p.Glu349del
NM_005345.5:c.1540_1542del (HSPA1A)	NP_005336.3:p.Glu514del
XM_005249073.2:c.-14+3720_-14+3722del (HSPA1L)	XP_005249130.1:n.-14+3720_-14+3722del
XM_011514566.1:c.-14+3720_-14+3722del (HSPA1L)	XP_011512868.1:n.-14+3720_-14+3722del
NM_005345.6:c.1540_1542del (HSPA1A) MANE Select	NP_005336.3:p.Glu514del