Canonical Allele Identifier: CA62854009

Gene: HSPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.197490433dup , CM000664.2:g.197490433dup	GRCh38
NC_000002.11:g.198355157dup , CM000664.1:g.198355157dup	GRCh37
NC_000002.10:g.198063402dup	NCBI36
NG_008915.1:g.14851dup

Transcript Alleles

HGVS	Amino-acid Change
NM_002156.5:c.870-128dup MANE Select	NP_002147.2:n.870-128dup
ENST00000388968.8:c.870-128dup MANE Select	ENSP00000373620.3:n.870-128dup
NM_002156.4:c.870-128dup	NP_002147.2:n.870-128dup
NM_199440.1:c.870-128dup	NP_955472.1:n.870-128dup
NM_199440.2:c.870-128dup	NP_955472.1:n.870-128dup
ENST00000345042.6:c.870-128dup	ENSP00000340019.2:n.870-128dup
ENST00000388968.7:c.870-128dup	ENSP00000373620.3:n.870-128dup
ENST00000418022.2:c.870-128dup	ENSP00000412227.2:n.870-128dup
ENST00000426480.2:c.870-128dup	ENSP00000414446.2:n.870-128dup
ENST00000428204.6:c.870-128dup	ENSP00000396460.2:n.870-128dup
ENST00000439605.2:c.870-128dup	ENSP00000402478.2:n.870-128dup
ENST00000440114.2:c.*676-128dup	ENSP00000390404.1:n.*676-128dup
ENST00000452200.6:c.870-128dup	ENSP00000412717.2:n.870-128dup
ENST00000461097.2:n.3618-128dup
ENST00000476746.6:n.1918-128dup
ENST00000491249.1:n.149dup
ENST00000676933.1:c.774-128dup	ENSP00000503144.1:n.774-128dup
ENST00000677403.1:c.870-128dup	ENSP00000504667.1:n.870-128dup
ENST00000677454.1:c.1007+103dup	ENSP00000503295.1:n.1007+103dup
ENST00000677792.1:c.870-1177dup	ENSP00000504645.1:n.870-1177dup
ENST00000677913.1:c.870-128dup	ENSP00000503139.1:n.870-128dup
ENST00000678170.1:c.597-128dup	ENSP00000503910.1:n.597-128dup
ENST00000678545.1:c.*179+103dup	ENSP00000502920.1:n.*179+103dup
ENST00000678621.1:c.870-128dup	ENSP00000504328.1:n.870-128dup
ENST00000678761.1:c.870-128dup	ENSP00000503894.1:n.870-128dup
ENST00000678969.1:n.1511-128dup
ENST00000679291.1:c.870-1177dup	ENSP00000504417.1:n.870-1177dup
XM_005246518.2:c.870-128dup	XP_005246575.1:n.870-128dup