Canonical Allele Identifier: CA334242
Gene: HSPD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 188178
dbSNP Id: rs149003485

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.197493399T>C , CM000664.2:g.197493399T>C GRCh38
NC_000002.11:g.198358123T>C , CM000664.1:g.198358123T>C GRCh37
NC_000002.10:g.198066368T>C NCBI36
NG_008915.1:g.11876A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000388968.8:c.794A>G MANE Select ENSP00000373620.3:p.Asn265Ser
ENST00000418022.2:c.794A>G ENSP00000412227.2:p.Asn265Ser
ENST00000426480.2:c.794A>G ENSP00000414446.2:p.Asn265Ser
ENST00000428204.6:c.794A>G ENSP00000396460.2:p.Asn265Ser
ENST00000439605.2:c.794A>G ENSP00000402478.2:p.Asn265Ser
ENST00000440114.2:c.*600A>G ENSP00000390404.1:n.*600A>G
ENST00000452200.6:c.794A>G ENSP00000412717.2:p.Asn265Ser
ENST00000461097.2:n.3542A>G
ENST00000476746.6:n.1842A>G
ENST00000676933.1:c.698A>G ENSP00000503144.1:p.Asn233Ser
ENST00000677403.1:c.794A>G ENSP00000504667.1:p.Asn265Ser
ENST00000677454.1:c.794A>G ENSP00000503295.1:p.Asn265Ser
ENST00000677792.1:c.794A>G ENSP00000504645.1:p.Asn265Ser
ENST00000677913.1:c.794A>G ENSP00000503139.1:p.Asn265Ser
ENST00000678170.1:c.521A>G ENSP00000503910.1:p.Asn174Ser
ENST00000678545.1:c.794A>G ENSP00000502920.1:p.Asn265Ser
ENST00000678621.1:c.794A>G ENSP00000504328.1:p.Asn265Ser
ENST00000678761.1:c.794A>G ENSP00000503894.1:p.Asn265Ser
ENST00000678969.1:n.1435A>G
ENST00000679291.1:c.794A>G ENSP00000504417.1:p.Asn265Ser
ENST00000345042.6:c.794A>G ENSP00000340019.2:p.Asn265Ser
ENST00000388968.7:c.794A>G ENSP00000373620.3:p.Asn265Ser
ENST00000482167.1:n.412A>G
NM_002156.4:c.794A>G NP_002147.2:p.Asn265Ser
NM_199440.1:c.794A>G NP_955472.1:p.Asn265Ser
XM_005246518.2:c.794A>G XP_005246575.1:p.Asn265Ser
NM_002156.5:c.794A>G MANE Select NP_002147.2:p.Asn265Ser
NM_199440.2:c.794A>G NP_955472.1:p.Asn265Ser