Canonical Allele Identifier: CA1878829972

Gene: HSPA5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.125238850G= , CM000671.2:g.125238850G=	GRCh38
NC_000009.11:g.128001129G= , CM000671.1:g.128001129G=	GRCh37
NC_000009.10:g.127040950G=	NCBI36
NG_027761.1:g.7538C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324460.7:c.997-23C= MANE Select	ENSP00000324173.6:n.997-23C=
ENST00000679355.1:n.1329C=
ENST00000679475.1:n.1581-23C=
ENST00000680032.1:c.997-23C=	ENSP00000506285.1:n.997-23C=
ENST00000680234.1:n.1253-23C=
ENST00000680257.1:n.1253-23C=
ENST00000680272.1:c.996+91C=	ENSP00000506097.1:n.996+91C=
ENST00000680494.1:n.2398C=
ENST00000680640.1:n.1948-23C=
ENST00000681045.1:n.1877-23C=
ENST00000681424.1:n.1329C=
ENST00000681540.1:n.1253-23C=
ENST00000681544.1:n.1328-23C=
ENST00000681675.1:n.1877-23C=
ENST00000681774.1:n.2219-23C=
ENST00000324460.6:c.997-23C=	ENSP00000324173.6:n.997-23C=
NM_005347.4:c.997-23C=	NP_005338.1:n.997-23C=
NM_005347.5:c.997-23C= MANE Select	NP_005338.1:n.997-23C=