Canonical Allele Identifier: CA2678043297
Gene: HSPA1A HGNC NCBI
HSPA1L HGNC NCBI

Linked Data

gnomAD v4: 6-31816425-CG-C
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31816429del , CM000668.2:g.31816429del GRCh38
NC_000006.11:g.31784206del , CM000668.1:g.31784206del GRCh37
NC_000006.10:g.31892185del NCBI36
NG_011855.1:g.3633del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375651.7:c.673del (HSPA1A) MANE Select ENSP00000364802.5:p.Asp225ThrfsTer14
ENST00000375651.6:c.673del (HSPA1A) ENSP00000364802.5:p.Asp225ThrfsTer14
ENST00000608703.1:c.178del (HSPA1A) ENSP00000477378.1:p.Asp60ThrfsTer14
NM_005345.5:c.673del (HSPA1A) NP_005336.3:p.Asp225ThrfsTer14
XM_005249073.2:c.-13-4441del (HSPA1L) XP_005249130.1:n.-13-4441del
XM_011514566.1:c.-13-4441del (HSPA1L) XP_011512868.1:n.-13-4441del
NM_005345.6:c.673del (HSPA1A) MANE Select NP_005336.3:p.Asp225ThrfsTer14
Search 100 bp 5'
Search 100 bp 3'