Canonical Allele Identifier: CA2770521537
Gene: HSPA1A HGNC NCBI
HSPA1L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31816858_31816859insAGAGTA , CM000668.2:g.31816858_31816859insAGAGTA GRCh38
NC_000006.11:g.31784635_31784636insAGAGTA , CM000668.1:g.31784635_31784636insAGAGTA GRCh37
NC_000006.10:g.31892614_31892615insAGAGTA NCBI36
NG_011855.1:g.3200_3201insTACTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000375651.7:c.1102_1103insAGAGTA (HSPA1A) MANE Select ENSP00000364802.5:p.Ala368delinsGluSerThr
ENST00000375651.6:c.1102_1103insAGAGTA (HSPA1A) ENSP00000364802.5:p.Ala368delinsGluSerThr
ENST00000608703.1:c.607_608insAGAGTA (HSPA1A) ENSP00000477378.1:p.Ala203delinsGluSerThr
NM_005345.5:c.1102_1103insAGAGTA (HSPA1A) NP_005336.3:p.Ala368delinsGluSerThr
XM_005249073.2:c.-14+4154_-14+4155insTACTCT (HSPA1L) XP_005249130.1:n.-14+4154_-14+4155insTACTCT
XM_011514566.1:c.-14+4154_-14+4155insTACTCT (HSPA1L) XP_011512868.1:n.-14+4154_-14+4155insTACTCT
NM_005345.6:c.1102_1103insAGAGTA (HSPA1A) MANE Select NP_005336.3:p.Ala368delinsGluSerThr