Canonical Allele Identifier: CA1619307544

Gene: HSPA1A HSPA1L

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31816863_31816866delinsGGCC , CM000668.2:g.31816863_31816866delinsGGCC	GRCh38
NC_000006.11:g.31784640_31784643delinsGGCC , CM000668.1:g.31784640_31784643delinsGGCC	GRCh37
NC_000006.10:g.31892619_31892622delinsGGCC	NCBI36
NG_011855.1:g.3193_3196delinsGGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375651.7:c.1107_1110delinsGGCC (HSPA1A) MANE Select	ENSP00000364802.5:p.Val369=
ENST00000375651.6:c.1107_1110delinsGGCC (HSPA1A)	ENSP00000364802.5:p.Val369=
ENST00000608703.1:c.612_615delinsGGCC (HSPA1A)	ENSP00000477378.1:p.Val204=
NM_005345.5:c.1107_1110delinsGGCC (HSPA1A)	NP_005336.3:p.Val369=
XM_005249073.2:c.-14+4147_-14+4150delinsGGCC (HSPA1L)	XP_005249130.1:n.-14+4147_-14+4150delinsGGCC
XM_011514566.1:c.-14+4147_-14+4150delinsGGCC (HSPA1L)	XP_011512868.1:n.-14+4147_-14+4150delinsGGCC
NM_005345.6:c.1107_1110delinsGGCC (HSPA1A) MANE Select	NP_005336.3:p.Val369=