Canonical Allele Identifier: CA1619307552

Gene: HSPA1A HSPA1L

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31816893_31816896delinsCCTG , CM000668.2:g.31816893_31816896delinsCCTG	GRCh38
NC_000006.11:g.31784670_31784673delinsCCTG , CM000668.1:g.31784670_31784673delinsCCTG	GRCh37
NC_000006.10:g.31892649_31892652delinsCCTG	NCBI36
NG_011855.1:g.3163_3166delinsCAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375651.7:c.1137_1140delinsCCTG (HSPA1A) MANE Select	ENSP00000364802.5:p.Ile379=
ENST00000375651.6:c.1137_1140delinsCCTG (HSPA1A)	ENSP00000364802.5:p.Ile379=
ENST00000608703.1:c.642_645delinsCCTG (HSPA1A)	ENSP00000477378.1:p.Ile214=
NM_005345.5:c.1137_1140delinsCCTG (HSPA1A)	NP_005336.3:p.Ile379=
XM_005249073.2:c.-14+4117_-14+4120delinsCAGG (HSPA1L)	XP_005249130.1:n.-14+4117_-14+4120delinsCAGG
XM_011514566.1:c.-14+4117_-14+4120delinsCAGG (HSPA1L)	XP_011512868.1:n.-14+4117_-14+4120delinsCAGG
NM_005345.6:c.1137_1140delinsCCTG (HSPA1A) MANE Select	NP_005336.3:p.Ile379=