Canonical Allele Identifier: CA1878829969
Gene: HSPA5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.125238844G= , CM000671.2:g.125238844G= GRCh38
NC_000009.11:g.128001123G= , CM000671.1:g.128001123G= GRCh37
NC_000009.10:g.127040944G= NCBI36
NG_027761.1:g.7544C=

Transcript Alleles

HGVS Amino-acid change
ENST00000324460.7:c.997-17C= MANE Select ENSP00000324173.6:n.997-17C=
ENST00000679355.1:n.1335C=
ENST00000679475.1:n.1581-17C=
ENST00000680032.1:c.997-17C= ENSP00000506285.1:n.997-17C=
ENST00000680234.1:n.1253-17C=
ENST00000680257.1:n.1253-17C=
ENST00000680272.1:c.996+97C= ENSP00000506097.1:n.996+97C=
ENST00000680494.1:n.2404C=
ENST00000680640.1:n.1948-17C=
ENST00000681045.1:n.1877-17C=
ENST00000681424.1:n.1335C=
ENST00000681540.1:n.1253-17C=
ENST00000681544.1:n.1328-17C=
ENST00000681675.1:n.1877-17C=
ENST00000681774.1:n.2219-17C=
ENST00000324460.6:c.997-17C= ENSP00000324173.6:n.997-17C=
NM_005347.4:c.997-17C= NP_005338.1:n.997-17C=
NM_005347.5:c.997-17C= MANE Select NP_005338.1:n.997-17C=