Canonical Allele Identifier: CA467209628

Gene: HSPA5

Linked Data

• MyVariant Identifiers: chr9:g.128001226G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.125238947G>T , CM000671.2:g.125238947G>T	GRCh38
NC_000009.11:g.128001226G>T , CM000671.1:g.128001226G>T	GRCh37
NC_000009.10:g.127041047G>T	NCBI36
NG_027761.1:g.7441C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324460.7:c.990C>A MANE Select	ENSP00000324173.6:p.Leu330=
ENST00000679355.1:n.1232C>A
ENST00000679475.1:n.1574C>A
ENST00000680032.1:c.990C>A	ENSP00000506285.1:p.Leu330=
ENST00000680234.1:n.1246C>A
ENST00000680257.1:n.1246C>A
ENST00000680272.1:c.990C>A	ENSP00000506097.1:p.Leu330=
ENST00000680494.1:n.2301C>A
ENST00000680640.1:n.1941C>A
ENST00000681045.1:n.1870C>A
ENST00000681424.1:n.1232C>A
ENST00000681540.1:n.1246C>A
ENST00000681544.1:n.1321C>A
ENST00000681675.1:n.1870C>A
ENST00000681774.1:n.2212C>A
ENST00000324460.6:c.990C>A	ENSP00000324173.6:p.Leu330=
NM_005347.4:c.990C>A	NP_005338.1:p.Leu330=
NM_005347.5:c.990C>A MANE Select	NP_005338.1:p.Leu330=