Canonical Allele Identifier: CA566692202

Gene: HSPA1A HSPA1L

Linked Data

• dbSNP Id: rs1281677893
• gnomAD v2: 6-31785009-CAA-C
• gnomAD v4: 6-31817232-CAA-C
• MyVariant Identifiers: chr6:g.31785010_31785011del (hg19) ; chr6:g.31817233_31817234del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31817233_31817234del , CM000668.2:g.31817233_31817234del	GRCh38
NC_000006.11:g.31785010_31785011del , CM000668.1:g.31785010_31785011del	GRCh37
NC_000006.10:g.31892989_31892990del	NCBI36
NG_011855.1:g.2825_2826del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375651.7:c.1477_1478del (HSPA1A) MANE Select	ENSP00000364802.5:p.Lys493GlufsTer?
ENST00000375651.6:c.1477_1478del (HSPA1A)	ENSP00000364802.5:p.Lys493GlufsTer?
ENST00000608703.1:c.982_983del (HSPA1A)	ENSP00000477378.1:p.Lys328GlufsTer?
NM_005345.5:c.1477_1478del (HSPA1A)	NP_005336.3:p.Lys493GlufsTer?
XM_005249073.2:c.-14+3779_-14+3780del (HSPA1L)	XP_005249130.1:n.-14+3779_-14+3780del
XM_011514566.1:c.-14+3779_-14+3780del (HSPA1L)	XP_011512868.1:n.-14+3779_-14+3780del
NM_005345.6:c.1477_1478del (HSPA1A) MANE Select	NP_005336.3:p.Lys493GlufsTer?