Canonical Allele Identifier: CA1319265819

Gene: HSPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.197489690T= , CM000664.2:g.197489690T=	GRCh38
NC_000002.11:g.198354414T= , CM000664.1:g.198354414T=	GRCh37
NC_000002.10:g.198062659T=	NCBI36
NG_008915.1:g.15585A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388968.8:c.970-443A= MANE Select	ENSP00000373620.3:n.970-443A=
ENST00000418022.2:c.970-443A=	ENSP00000412227.2:n.970-443A=
ENST00000426480.2:c.970-443A=	ENSP00000414446.2:n.970-443A=
ENST00000428204.6:c.970-443A=	ENSP00000396460.2:n.970-443A=
ENST00000439605.2:c.970-443A=	ENSP00000402478.2:n.970-443A=
ENST00000440114.2:c.*776-443A=	ENSP00000390404.1:n.*776-443A=
ENST00000452200.6:c.970-443A=	ENSP00000412717.2:n.970-443A=
ENST00000461097.2:n.3718-443A=
ENST00000476746.6:n.2018-443A=
ENST00000676933.1:c.874-443A=	ENSP00000503144.1:n.874-443A=
ENST00000677403.1:c.1093+40A=	ENSP00000504667.1:n.1093+40A=
ENST00000677454.1:c.1108-443A=	ENSP00000503295.1:n.1108-443A=
ENST00000677792.1:c.870-443A=	ENSP00000504645.1:n.870-443A=
ENST00000677913.1:c.970-443A=	ENSP00000503139.1:n.970-443A=
ENST00000678170.1:c.697-443A=	ENSP00000503910.1:n.697-443A=
ENST00000678545.1:c.*280-443A=	ENSP00000502920.1:n.*280-443A=
ENST00000678621.1:c.970-443A=	ENSP00000504328.1:n.970-443A=
ENST00000678761.1:c.970-443A=	ENSP00000503894.1:n.970-443A=
ENST00000678969.1:n.2117A=
ENST00000679291.1:c.870-443A=	ENSP00000504417.1:n.870-443A=
ENST00000345042.6:c.970-443A=	ENSP00000340019.2:n.970-443A=
ENST00000388968.7:c.970-443A=	ENSP00000373620.3:n.970-443A=
ENST00000491249.1:n.377-443A=
NM_002156.4:c.970-443A=	NP_002147.2:n.970-443A=
NM_199440.1:c.970-443A=	NP_955472.1:n.970-443A=
XM_005246518.2:c.970-443A=	XP_005246575.1:n.970-443A=
NM_002156.5:c.970-443A= MANE Select	NP_002147.2:n.970-443A=
NM_199440.2:c.970-443A=	NP_955472.1:n.970-443A=