Canonical Allele Identifier: CA1319309788

Gene: HSPE1 HSPD1 HSPE1-MOB4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.197501089A= , CM000664.2:g.197501089A=	GRCh38
NC_000002.11:g.198365813A= , CM000664.1:g.198365813A=	GRCh37
NC_000002.10:g.198074058A=	NCBI36
NG_008914.1:g.6093A=
NG_008915.1:g.4186T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233893.10:c.19A= (HSPE1) MANE Select	ENSP00000233893.5:p.Arg7=
ENST00000426480.2:c.-2-2239T= (HSPD1)	ENSP00000414446.2:n.-2-2239T=
ENST00000233893.9:c.19A= (HSPE1)	ENSP00000233893.5:p.Arg7=
ENST00000409468.1:c.19A= (HSPE1)	ENSP00000386447.1:p.Arg7=
ENST00000409729.1:c.3+650A= (HSPE1)	ENSP00000387101.1:n.3+650A=
ENST00000426480.1:c.125-2239T= (HSPD1)	ENSP00000414446.1:n.125-2239T=
ENST00000463841.1:n.208A= (HSPE1)
ENST00000465573.1:n.376+171A= (HSPE1)
ENST00000473395.1:n.107A= (HSPE1)
ENST00000495200.1:n.497A= (HSPE1)
ENST00000604458.1:c.19A= (HSPE1-MOB4)	ENSP00000474534.1:p.Arg7=
NM_001202485.1:c.19A= (HSPE1-MOB4)	NP_001189414.1:p.Arg7=
NM_002157.2:c.19A= (HSPE1)	NP_002148.1:p.Arg7=
NM_002157.3:c.19A= (HSPE1) MANE Select	NP_002148.1:p.Arg7=
NM_001202485.2:c.19A= (HSPE1-MOB4)	NP_001189414.1:p.Arg7=