Canonical Allele Identifier: CA2678045961

Gene: HSPA1A HSPA1L

Linked Data

• gnomAD v4: 6-31817224-G-GCCACGGACAAGAGC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31817225_31817238dup , CM000668.2:g.31817225_31817238dup	GRCh38
NC_000006.11:g.31785002_31785015dup , CM000668.1:g.31785002_31785015dup	GRCh37
NC_000006.10:g.31892981_31892994dup	NCBI36
NG_011855.1:g.2821_2834dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375651.7:c.1469_1482dup (HSPA1A) MANE Select	ENSP00000364802.5:p.Thr495ProfsTer21
ENST00000375651.6:c.1469_1482dup (HSPA1A)	ENSP00000364802.5:p.Thr495ProfsTer21
ENST00000608703.1:c.974_987dup (HSPA1A)	ENSP00000477378.1:p.Thr330ProfsTer21
NM_005345.5:c.1469_1482dup (HSPA1A)	NP_005336.3:p.Thr495ProfsTer21
XM_005249073.2:c.-14+3775_-14+3788dup (HSPA1L)	XP_005249130.1:n.-14+3775_-14+3788dup
XM_011514566.1:c.-14+3775_-14+3788dup (HSPA1L)	XP_011512868.1:n.-14+3775_-14+3788dup
NM_005345.6:c.1469_1482dup (HSPA1A) MANE Select	NP_005336.3:p.Thr495ProfsTer21