Canonical Allele Identifier: CA2770521539

Gene: HSPA1A HSPA1L

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31816899_31816903del , CM000668.2:g.31816899_31816903del	GRCh38
NC_000006.11:g.31784676_31784680del , CM000668.1:g.31784676_31784680del	GRCh37
NC_000006.10:g.31892655_31892659del	NCBI36
NG_011855.1:g.3156_3160del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375651.7:c.1143_1147del (HSPA1A) MANE Select	ENSP00000364802.5:p.Met381IlefsTer?
ENST00000375651.6:c.1143_1147del (HSPA1A)	ENSP00000364802.5:p.Met381IlefsTer?
ENST00000608703.1:c.648_652del (HSPA1A)	ENSP00000477378.1:p.Met216IlefsTer?
NM_005345.5:c.1143_1147del (HSPA1A)	NP_005336.3:p.Met381IlefsTer?
XM_005249073.2:c.-14+4110_-14+4114del (HSPA1L)	XP_005249130.1:n.-14+4110_-14+4114del
XM_011514566.1:c.-14+4110_-14+4114del (HSPA1L)	XP_011512868.1:n.-14+4110_-14+4114del
NM_005345.6:c.1143_1147del (HSPA1A) MANE Select	NP_005336.3:p.Met381IlefsTer?