Canonical Allele Identifier: CA566692224

Gene: HSPA1A HSPA1L

Linked Data

• dbSNP Id: rs1214778976
• gnomAD v2: 6-31784670-CCTG-C
• gnomAD v4: 6-31816893-CCTG-C
• MyVariant Identifiers: chr6:g.31784671_31784673del (hg19) ; chr6:g.31816894_31816896del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31816894_31816896del , CM000668.2:g.31816894_31816896del	GRCh38
NC_000006.11:g.31784671_31784673del , CM000668.1:g.31784671_31784673del	GRCh37
NC_000006.10:g.31892650_31892652del	NCBI36
NG_011855.1:g.3163_3165del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375651.7:c.1138_1140del (HSPA1A) MANE Select	ENSP00000364802.5:p.Leu380del
ENST00000375651.6:c.1138_1140del (HSPA1A)	ENSP00000364802.5:p.Leu380del
ENST00000608703.1:c.643_645del (HSPA1A)	ENSP00000477378.1:p.Leu215del
NM_005345.5:c.1138_1140del (HSPA1A)	NP_005336.3:p.Leu380del
XM_005249073.2:c.-14+4117_-14+4119del (HSPA1L)	XP_005249130.1:n.-14+4117_-14+4119del
XM_011514566.1:c.-14+4117_-14+4119del (HSPA1L)	XP_011512868.1:n.-14+4117_-14+4119del
NM_005345.6:c.1138_1140del (HSPA1A) MANE Select	NP_005336.3:p.Leu380del