Canonical Allele Identifier: CA1619307601

Gene: HSPA1A HSPA1L

Linked Data

• dbSNP Id: rs1815980210

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31817189_31817190insG , CM000668.2:g.31817189_31817190insG	GRCh38
NC_000006.11:g.31784966_31784967insG , CM000668.1:g.31784966_31784967insG	GRCh37
NC_000006.10:g.31892945_31892946insG	NCBI36
NG_011855.1:g.2869_2870insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375651.7:c.1433_1434insG (HSPA1A) MANE Select	ENSP00000364802.5:p.Phe478LeufsTer?
ENST00000375651.6:c.1433_1434insG (HSPA1A)	ENSP00000364802.5:p.Phe478LeufsTer?
ENST00000608703.1:c.938_939insG (HSPA1A)	ENSP00000477378.1:p.Phe313LeufsTer?
NM_005345.5:c.1433_1434insG (HSPA1A)	NP_005336.3:p.Phe478LeufsTer?
XM_005249073.2:c.-14+3823_-14+3824insC (HSPA1L)	XP_005249130.1:n.-14+3823_-14+3824insC
XM_011514566.1:c.-14+3823_-14+3824insC (HSPA1L)	XP_011512868.1:n.-14+3823_-14+3824insC
NM_005345.6:c.1433_1434insG (HSPA1A) MANE Select	NP_005336.3:p.Phe478LeufsTer?