Canonical Allele Identifier: CA1619307575

Gene: HSPA1A HSPA1L

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31817085_31817093delinsCGAGGGCGA , CM000668.2:g.31817085_31817093delinsCGAGGGCGA	GRCh38
NC_000006.11:g.31784862_31784870delinsCGAGGGCGA , CM000668.1:g.31784862_31784870delinsCGAGGGCGA	GRCh37
NC_000006.10:g.31892841_31892849delinsCGAGGGCGA	NCBI36
NG_011855.1:g.2966_2974delinsTCGCCCTCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375651.7:c.1329_1337delinsCGAGGGCGA (HSPA1A) MANE Select	ENSP00000364802.5:p.Tyr443=
ENST00000375651.6:c.1329_1337delinsCGAGGGCGA (HSPA1A)	ENSP00000364802.5:p.Tyr443=
ENST00000608703.1:c.834_842delinsCGAGGGCGA (HSPA1A)	ENSP00000477378.1:p.Tyr278=
NM_005345.5:c.1329_1337delinsCGAGGGCGA (HSPA1A)	NP_005336.3:p.Tyr443=
XM_005249073.2:c.-14+3920_-14+3928delinsTCGCCCTCG (HSPA1L)	XP_005249130.1:n.-14+3920_-14+3928delinsTCGCCCTCG
XM_011514566.1:c.-14+3920_-14+3928delinsTCGCCCTCG (HSPA1L)	XP_011512868.1:n.-14+3920_-14+3928delinsTCGCCCTCG
NM_005345.6:c.1329_1337delinsCGAGGGCGA (HSPA1A) MANE Select	NP_005336.3:p.Tyr443=