Canonical Allele Identifier: CA1319331393
Gene: HSPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.197487376G= , CM000664.2:g.197487376G= GRCh38
NC_000002.11:g.198352100G= , CM000664.1:g.198352100G= GRCh37
NC_000002.10:g.198060345G= NCBI36
NG_008915.1:g.17899C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000388968.8:c.1570-178C= MANE Select ENSP00000373620.3:n.1570-178C=
ENST00000418022.2:c.1570-178C= ENSP00000412227.2:n.1570-178C=
ENST00000426480.2:c.1570-178C= ENSP00000414446.2:n.1570-178C=
ENST00000428204.6:c.1570-178C= ENSP00000396460.2:n.1570-178C=
ENST00000439605.2:c.1570-178C= ENSP00000402478.2:n.1570-178C=
ENST00000440114.2:c.*1376-178C= ENSP00000390404.1:n.*1376-178C=
ENST00000452200.6:c.1570-178C= ENSP00000412717.2:n.1570-178C=
ENST00000461097.2:n.4318-178C=
ENST00000476746.6:n.2618-178C=
ENST00000676933.1:c.1474-178C= ENSP00000503144.1:n.1474-178C=
ENST00000677403.1:c.*566-178C= ENSP00000504667.1:n.*566-178C=
ENST00000677454.1:c.1708-178C= ENSP00000503295.1:n.1708-178C=
ENST00000677792.1:c.*579-178C= ENSP00000504645.1:n.*579-178C=
ENST00000677913.1:c.1570-178C= ENSP00000503139.1:n.1570-178C=
ENST00000678170.1:c.1297-178C= ENSP00000503910.1:n.1297-178C=
ENST00000678545.1:c.*880-178C= ENSP00000502920.1:n.*880-178C=
ENST00000678621.1:c.1573C= ENSP00000504328.1:p.Arg525=
ENST00000678761.1:c.1570-178C= ENSP00000503894.1:n.1570-178C=
ENST00000678969.1:n.3160-178C=
ENST00000679291.1:c.*579-178C= ENSP00000504417.1:n.*579-178C=
ENST00000345042.6:c.1570-178C= ENSP00000340019.2:n.1570-178C=
ENST00000388968.7:c.1570-178C= ENSP00000373620.3:n.1570-178C=
NM_002156.4:c.1570-178C= NP_002147.2:n.1570-178C=
NM_199440.1:c.1570-178C= NP_955472.1:n.1570-178C=
XM_005246518.2:c.1570-178C= XP_005246575.1:n.1570-178C=
NM_002156.5:c.1570-178C= MANE Select NP_002147.2:n.1570-178C=
NM_199440.2:c.1570-178C= NP_955472.1:n.1570-178C=