Canonical Allele Identifier: CA449806583

Gene: HSPA1A HSPA1L

Linked Data

• dbSNP Id: rs1180346249
• gnomAD v3: 6-31817217-C-T
• gnomAD v4: 6-31817217-C-T
• MyVariant Identifiers: chr6:g.31784994C>T (hg19) ; chr6:g.31817217C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31817217C>T , CM000668.2:g.31817217C>T	GRCh38
NC_000006.11:g.31784994C>T , CM000668.1:g.31784994C>T	GRCh37
NC_000006.10:g.31892973C>T	NCBI36
NG_011855.1:g.2842G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375651.7:c.1461C>T (HSPA1A) MANE Select	ENSP00000364802.5:p.Asn487=
ENST00000375651.6:c.1461C>T (HSPA1A)	ENSP00000364802.5:p.Asn487=
ENST00000608703.1:c.966C>T (HSPA1A)	ENSP00000477378.1:p.Asn322=
NM_005345.5:c.1461C>T (HSPA1A)	NP_005336.3:p.Asn487=
XM_005249073.2:c.-14+3796G>A (HSPA1L)	XP_005249130.1:n.-14+3796G>A
XM_011514566.1:c.-14+3796G>A (HSPA1L)	XP_011512868.1:n.-14+3796G>A
NM_005345.6:c.1461C>T (HSPA1A) MANE Select	NP_005336.3:p.Asn487=