Canonical Allele Identifier: CA2691675869

Gene: HSPA5

Linked Data

• gnomAD v4: 9-125238843-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.125238843G>T , CM000671.2:g.125238843G>T	GRCh38
NC_000009.11:g.128001122G>T , CM000671.1:g.128001122G>T	GRCh37
NC_000009.10:g.127040943G>T	NCBI36
NG_027761.1:g.7545C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000324460.7:c.997-16C>A MANE Select	ENSP00000324173.6:n.997-16C>A
ENST00000679355.1:n.1336C>A
ENST00000679475.1:n.1581-16C>A
ENST00000680032.1:c.997-16C>A	ENSP00000506285.1:n.997-16C>A
ENST00000680234.1:n.1253-16C>A
ENST00000680257.1:n.1253-16C>A
ENST00000680272.1:c.996+98C>A	ENSP00000506097.1:n.996+98C>A
ENST00000680494.1:n.2405C>A
ENST00000680640.1:n.1948-16C>A
ENST00000681045.1:n.1877-16C>A
ENST00000681424.1:n.1336C>A
ENST00000681540.1:n.1253-16C>A
ENST00000681544.1:n.1328-16C>A
ENST00000681675.1:n.1877-16C>A
ENST00000681774.1:n.2219-16C>A
ENST00000324460.6:c.997-16C>A	ENSP00000324173.6:n.997-16C>A
NM_005347.4:c.997-16C>A	NP_005338.1:n.997-16C>A
NM_005347.5:c.997-16C>A MANE Select	NP_005338.1:n.997-16C>A