Canonical Allele Identifier: CA2678044536
Gene: HSPA1A HGNC NCBI
HSPA1L HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31816857_31816858insCCAGAA , CM000668.2:g.31816857_31816858insCCAGAA GRCh38
NC_000006.11:g.31784634_31784635insCCAGAA , CM000668.1:g.31784634_31784635insCCAGAA GRCh37
NC_000006.10:g.31892613_31892614insCCAGAA NCBI36
NG_011855.1:g.3201_3202insTTCTGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000375651.7:c.1101_1102insCCAGAA (HSPA1A) MANE Select ENSP00000364802.5:p.Glu367_Ala368insProGlu
ENST00000375651.6:c.1101_1102insCCAGAA (HSPA1A) ENSP00000364802.5:p.Glu367_Ala368insProGlu
ENST00000608703.1:c.606_607insCCAGAA (HSPA1A) ENSP00000477378.1:p.Glu202_Ala203insProGlu
NM_005345.5:c.1101_1102insCCAGAA (HSPA1A) NP_005336.3:p.Glu367_Ala368insProGlu
XM_005249073.2:c.-14+4155_-14+4156insTTCTGG (HSPA1L) XP_005249130.1:n.-14+4155_-14+4156insTTCTGG
XM_011514566.1:c.-14+4155_-14+4156insTTCTGG (HSPA1L) XP_011512868.1:n.-14+4155_-14+4156insTTCTGG
NM_005345.6:c.1101_1102insCCAGAA (HSPA1A) MANE Select NP_005336.3:p.Glu367_Ala368insProGlu