Canonical Allele Identifier: CA2844078117
Gene: HSPA1A HGNC NCBI
HSPA1L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31816731del , CM000668.2:g.31816731del GRCh38
NC_000006.11:g.31784508del , CM000668.1:g.31784508del GRCh37
NC_000006.10:g.31892487del NCBI36
NG_011855.1:g.3328del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375651.7:c.975del (HSPA1A) MANE Select ENSP00000364802.5:p.Lys325AsnfsTer?
ENST00000375651.6:c.975del (HSPA1A) ENSP00000364802.5:p.Lys325AsnfsTer?
ENST00000608703.1:c.480del (HSPA1A) ENSP00000477378.1:p.Lys160AsnfsTer?
NM_005345.5:c.975del (HSPA1A) NP_005336.3:p.Lys325AsnfsTer?
XM_005249073.2:c.-14+4282del (HSPA1L) XP_005249130.1:n.-14+4282del
XM_011514566.1:c.-14+4282del (HSPA1L) XP_011512868.1:n.-14+4282del
NM_005345.6:c.975del (HSPA1A) MANE Select NP_005336.3:p.Lys325AsnfsTer?