Canonical Allele Identifier: CA363418062

Gene: HSPA1A HSPA1L

Linked Data

• dbSNP Id: rs1178742095
• gnomAD v2: 6-31784935-C-T
• gnomAD v4: 6-31817158-C-T
• MyVariant Identifiers: chr6:g.31784935C>T (hg19) ; chr6:g.31817158C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31817158C>T , CM000668.2:g.31817158C>T	GRCh38
NC_000006.11:g.31784935C>T , CM000668.1:g.31784935C>T	GRCh37
NC_000006.10:g.31892914C>T	NCBI36
NG_011855.1:g.2901G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375651.7:c.1402C>T (HSPA1A) MANE Select	ENSP00000364802.5:p.Pro468Ser
ENST00000375651.6:c.1402C>T (HSPA1A)	ENSP00000364802.5:p.Pro468Ser
ENST00000608703.1:c.907C>T (HSPA1A)	ENSP00000477378.1:p.Pro303Ser
NM_005345.5:c.1402C>T (HSPA1A)	NP_005336.3:p.Pro468Ser
XM_005249073.2:c.-14+3855G>A (HSPA1L)	XP_005249130.1:n.-14+3855G>A
XM_011514566.1:c.-14+3855G>A (HSPA1L)	XP_011512868.1:n.-14+3855G>A
NM_005345.6:c.1402C>T (HSPA1A) MANE Select	NP_005336.3:p.Pro468Ser