Canonical Allele Identifier: CA1139657585

Gene: HSPD1

Linked Data

• ClinVar Variation Id: 895969
• ClinVar RCV Id: RCV001138359
• dbSNP Id: rs2086032939

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.197486925A>G , CM000664.2:g.197486925A>G	GRCh38
NC_000002.11:g.198351649A>G , CM000664.1:g.198351649A>G	GRCh37
NC_000002.10:g.198059894A>G	NCBI36
NG_008915.1:g.18350T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388968.8:c.*121T>C MANE Select	ENSP00000373620.3:n.*121T>C
ENST00000418022.2:c.*121T>C	ENSP00000412227.2:n.*121T>C
ENST00000426480.2:c.*121T>C	ENSP00000414446.2:n.*121T>C
ENST00000428204.6:c.*121T>C	ENSP00000396460.2:n.*121T>C
ENST00000439605.2:c.*121T>C	ENSP00000402478.2:n.*121T>C
ENST00000440114.2:c.*1649T>C	ENSP00000390404.1:n.*1649T>C
ENST00000452200.6:c.*121T>C	ENSP00000412717.2:n.*121T>C
ENST00000461097.2:n.4591T>C
ENST00000476746.6:n.2891T>C
ENST00000676933.1:c.*121T>C	ENSP00000503144.1:n.*121T>C
ENST00000677403.1:c.*839T>C	ENSP00000504667.1:n.*839T>C
ENST00000677454.1:c.1981T>C	ENSP00000503295.1:n.1981T>C
ENST00000677792.1:c.*852T>C	ENSP00000504645.1:n.*852T>C
ENST00000677913.1:c.*121T>C	ENSP00000503139.1:n.*121T>C
ENST00000678170.1:c.*121T>C	ENSP00000503910.1:n.*121T>C
ENST00000678545.1:c.*1153T>C	ENSP00000502920.1:n.*1153T>C
ENST00000678621.1:c.*321T>C	ENSP00000504328.1:n.*321T>C
ENST00000678761.1:c.*121T>C	ENSP00000503894.1:n.*121T>C
ENST00000678969.1:n.3433T>C
ENST00000679291.1:c.*852T>C	ENSP00000504417.1:n.*852T>C
ENST00000345042.6:c.*121T>C	ENSP00000340019.2:n.*121T>C
ENST00000388968.7:c.*121T>C	ENSP00000373620.3:n.*121T>C
NM_002156.4:c.*121T>C	NP_002147.2:n.*121T>C
NM_199440.1:c.*121T>C	NP_955472.1:n.*121T>C
XM_005246518.2:c.*121T>C	XP_005246575.1:n.*121T>C
NM_002156.5:c.*121T>C MANE Select	NP_002147.2:n.*121T>C
NM_199440.2:c.*121T>C	NP_955472.1:n.*121T>C