Canonical Allele Identifier: CA2691675875

Gene: HSPA5

Linked Data

• gnomAD v4: 9-125238861-T-TATCTA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.125238863_125238867dup , CM000671.2:g.125238863_125238867dup	GRCh38
NC_000009.11:g.128001142_128001146dup , CM000671.1:g.128001142_128001146dup	GRCh37
NC_000009.10:g.127040963_127040967dup	NCBI36
NG_027761.1:g.7522_7526dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000324460.7:c.997-39_997-35dup MANE Select	ENSP00000324173.6:n.997-39_997-35dup
ENST00000679355.1:n.1313_1317dup
ENST00000679475.1:n.1581-39_1581-35dup
ENST00000680032.1:c.997-39_997-35dup	ENSP00000506285.1:n.997-39_997-35dup
ENST00000680234.1:n.1253-39_1253-35dup
ENST00000680257.1:n.1253-39_1253-35dup
ENST00000680272.1:c.996+75_996+79dup	ENSP00000506097.1:n.996+75_996+79dup
ENST00000680494.1:n.2382_2386dup
ENST00000680640.1:n.1948-39_1948-35dup
ENST00000681045.1:n.1877-39_1877-35dup
ENST00000681424.1:n.1313_1317dup
ENST00000681540.1:n.1253-39_1253-35dup
ENST00000681544.1:n.1328-39_1328-35dup
ENST00000681675.1:n.1877-39_1877-35dup
ENST00000681774.1:n.2219-39_2219-35dup
ENST00000324460.6:c.997-39_997-35dup	ENSP00000324173.6:n.997-39_997-35dup
NM_005347.4:c.997-39_997-35dup	NP_005338.1:n.997-39_997-35dup
NM_005347.5:c.997-39_997-35dup MANE Select	NP_005338.1:n.997-39_997-35dup