Canonical Allele Identifier: CA2043352

Gene: HSPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.197487939T>C , CM000664.2:g.197487939T>C	GRCh38
NC_000002.11:g.198352663T>C , CM000664.1:g.198352663T>C	GRCh37
NC_000002.10:g.198060908T>C	NCBI36
NG_008915.1:g.17336A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388968.8:c.1488A>G MANE Select	ENSP00000373620.3:p.Gln496=
ENST00000418022.2:c.1488A>G	ENSP00000412227.2:p.Gln496=
ENST00000426480.2:c.1488A>G	ENSP00000414446.2:p.Gln496=
ENST00000428204.6:c.1488A>G	ENSP00000396460.2:p.Gln496=
ENST00000439605.2:c.1488A>G	ENSP00000402478.2:p.Gln496=
ENST00000440114.2:c.*1294A>G	ENSP00000390404.1:n.*1294A>G
ENST00000452200.6:c.1488A>G	ENSP00000412717.2:p.Gln496=
ENST00000461097.2:n.4236A>G
ENST00000476746.6:n.2536A>G
ENST00000676933.1:c.1392A>G	ENSP00000503144.1:p.Gln464=
ENST00000677403.1:c.*484A>G	ENSP00000504667.1:n.*484A>G
ENST00000677454.1:c.1626A>G	ENSP00000503295.1:n.1626A>G
ENST00000677792.1:c.*497A>G	ENSP00000504645.1:n.*497A>G
ENST00000677913.1:c.1488A>G	ENSP00000503139.1:p.Gln496=
ENST00000678170.1:c.1215A>G	ENSP00000503910.1:p.Gln405=
ENST00000678545.1:c.*798A>G	ENSP00000502920.1:n.*798A>G
ENST00000678621.1:c.1488A>G	ENSP00000504328.1:p.Gln496=
ENST00000678761.1:c.1488A>G	ENSP00000503894.1:p.Gln496=
ENST00000678969.1:n.3078A>G
ENST00000679291.1:c.*497A>G	ENSP00000504417.1:n.*497A>G
ENST00000345042.6:c.1488A>G	ENSP00000340019.2:p.Gln496=
ENST00000388968.7:c.1488A>G	ENSP00000373620.3:p.Gln496=
NM_002156.4:c.1488A>G	NP_002147.2:p.Gln496=
NM_199440.1:c.1488A>G	NP_955472.1:p.Gln496=
XM_005246518.2:c.1488A>G	XP_005246575.1:p.Gln496=
NM_002156.5:c.1488A>G MANE Select	NP_002147.2:p.Gln496=
NM_199440.2:c.1488A>G	NP_955472.1:p.Gln496=