Canonical Allele Identifier: CA2691675874

Gene: HSPA5

Linked Data

• gnomAD v4: 9-125238861-T-TGA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.125238861_125238862insGA , CM000671.2:g.125238861_125238862insGA	GRCh38
NC_000009.11:g.128001140_128001141insGA , CM000671.1:g.128001140_128001141insGA	GRCh37
NC_000009.10:g.127040961_127040962insGA	NCBI36
NG_027761.1:g.7526_7527insTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000324460.7:c.997-35_997-34insTC MANE Select	ENSP00000324173.6:n.997-35_997-34insTC
ENST00000679355.1:n.1317_1318insTC
ENST00000679475.1:n.1581-35_1581-34insTC
ENST00000680032.1:c.997-35_997-34insTC	ENSP00000506285.1:n.997-35_997-34insTC
ENST00000680234.1:n.1253-35_1253-34insTC
ENST00000680257.1:n.1253-35_1253-34insTC
ENST00000680272.1:c.996+79_996+80insTC	ENSP00000506097.1:n.996+79_996+80insTC
ENST00000680494.1:n.2386_2387insTC
ENST00000680640.1:n.1948-35_1948-34insTC
ENST00000681045.1:n.1877-35_1877-34insTC
ENST00000681424.1:n.1317_1318insTC
ENST00000681540.1:n.1253-35_1253-34insTC
ENST00000681544.1:n.1328-35_1328-34insTC
ENST00000681675.1:n.1877-35_1877-34insTC
ENST00000681774.1:n.2219-35_2219-34insTC
ENST00000324460.6:c.997-35_997-34insTC	ENSP00000324173.6:n.997-35_997-34insTC
NM_005347.4:c.997-35_997-34insTC	NP_005338.1:n.997-35_997-34insTC
NM_005347.5:c.997-35_997-34insTC MANE Select	NP_005338.1:n.997-35_997-34insTC