Canonical Allele Identifier: CA2678044594

Gene: HSPA1A HSPA1L

Linked Data

• gnomAD v4: 6-31816867-TACGGGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31816868_31816873del , CM000668.2:g.31816868_31816873del	GRCh38
NC_000006.11:g.31784645_31784650del , CM000668.1:g.31784645_31784650del	GRCh37
NC_000006.10:g.31892624_31892629del	NCBI36
NG_011855.1:g.3186_3191del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375651.7:c.1112_1117del (HSPA1A) MANE Select	ENSP00000364802.5:p.Tyr371_Ala373delinsSer
ENST00000375651.6:c.1112_1117del (HSPA1A)	ENSP00000364802.5:p.Tyr371_Ala373delinsSer
ENST00000608703.1:c.617_622del (HSPA1A)	ENSP00000477378.1:p.Tyr206_Ala208delinsSer
NM_005345.5:c.1112_1117del (HSPA1A)	NP_005336.3:p.Tyr371_Ala373delinsSer
XM_005249073.2:c.-14+4140_-14+4145del (HSPA1L)	XP_005249130.1:n.-14+4140_-14+4145del
XM_011514566.1:c.-14+4140_-14+4145del (HSPA1L)	XP_011512868.1:n.-14+4140_-14+4145del
NM_005345.6:c.1112_1117del (HSPA1A) MANE Select	NP_005336.3:p.Tyr371_Ala373delinsSer