Canonical Allele Identifier: CA762964216
Gene: HSPD1 HGNC NCBI

Linked Data

dbSNP Id: rs1356775928

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.197487550_197487552dup , CM000664.2:g.197487550_197487552dup GRCh38
NC_000002.11:g.198352274_198352276dup , CM000664.1:g.198352274_198352276dup GRCh37
NC_000002.10:g.198060519_198060521dup NCBI36
NG_008915.1:g.17724_17726dup

Transcript Alleles

HGVS Amino-acid change
ENST00000388968.8:c.1569+307_1569+309dup MANE Select ENSP00000373620.3:n.1569+307_1569+309dup
ENST00000418022.2:c.1569+307_1569+309dup ENSP00000412227.2:n.1569+307_1569+309dup
ENST00000426480.2:c.1569+307_1569+309dup ENSP00000414446.2:n.1569+307_1569+309dup
ENST00000428204.6:c.1569+307_1569+309dup ENSP00000396460.2:n.1569+307_1569+309dup
ENST00000439605.2:c.1569+307_1569+309dup ENSP00000402478.2:n.1569+307_1569+309dup
ENST00000440114.2:c.*1375+307_*1375+309dup ENSP00000390404.1:n.*1375+307_*1375+309dup
ENST00000452200.6:c.1569+307_1569+309dup ENSP00000412717.2:n.1569+307_1569+309dup
ENST00000461097.2:n.4317+307_4317+309dup
ENST00000476746.6:n.2617+307_2617+309dup
ENST00000676933.1:c.1473+307_1473+309dup ENSP00000503144.1:n.1473+307_1473+309dup
ENST00000677403.1:c.*565+307_*565+309dup ENSP00000504667.1:n.*565+307_*565+309dup
ENST00000677454.1:c.1707+307_1707+309dup ENSP00000503295.1:n.1707+307_1707+309dup
ENST00000677792.1:c.*578+307_*578+309dup ENSP00000504645.1:n.*578+307_*578+309dup
ENST00000677913.1:c.1569+307_1569+309dup ENSP00000503139.1:n.1569+307_1569+309dup
ENST00000678170.1:c.1296+307_1296+309dup ENSP00000503910.1:n.1296+307_1296+309dup
ENST00000678545.1:c.*879+307_*879+309dup ENSP00000502920.1:n.*879+307_*879+309dup
ENST00000678621.1:c.1570-172_1570-170dup ENSP00000504328.1:n.1570-172_1570-170dup
ENST00000678761.1:c.1569+307_1569+309dup ENSP00000503894.1:n.1569+307_1569+309dup
ENST00000678969.1:n.3159+307_3159+309dup
ENST00000679291.1:c.*578+307_*578+309dup ENSP00000504417.1:n.*578+307_*578+309dup
ENST00000345042.6:c.1569+307_1569+309dup ENSP00000340019.2:n.1569+307_1569+309dup
ENST00000388968.7:c.1569+307_1569+309dup ENSP00000373620.3:n.1569+307_1569+309dup
NM_002156.4:c.1569+307_1569+309dup NP_002147.2:n.1569+307_1569+309dup
NM_199440.1:c.1569+307_1569+309dup NP_955472.1:n.1569+307_1569+309dup
XM_005246518.2:c.1569+307_1569+309dup XP_005246575.1:n.1569+307_1569+309dup
NM_002156.5:c.1569+307_1569+309dup MANE Select NP_002147.2:n.1569+307_1569+309dup
NM_199440.2:c.1569+307_1569+309dup NP_955472.1:n.1569+307_1569+309dup