Canonical Allele Identifier: CA430561952

Gene: HSPE1 HSPD1 HSPE1-MOB4

Linked Data

• MyVariant Identifiers: chr2:g.198365815A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.197501091A>G , CM000664.2:g.197501091A>G	GRCh38
NC_000002.11:g.198365815A>G , CM000664.1:g.198365815A>G	GRCh37
NC_000002.10:g.198074060A>G	NCBI36
NG_008914.1:g.6095A>G
NG_008915.1:g.4184T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233893.10:c.21A>G (HSPE1) MANE Select	ENSP00000233893.5:p.Arg7=
ENST00000426480.2:c.-2-2241T>C (HSPD1)	ENSP00000414446.2:n.-2-2241T>C
ENST00000233893.9:c.21A>G (HSPE1)	ENSP00000233893.5:p.Arg7=
ENST00000409468.1:c.21A>G (HSPE1)	ENSP00000386447.1:p.Arg7=
ENST00000409729.1:c.3+652A>G (HSPE1)	ENSP00000387101.1:n.3+652A>G
ENST00000426480.1:c.125-2241T>C (HSPD1)	ENSP00000414446.1:n.125-2241T>C
ENST00000463841.1:n.210A>G (HSPE1)
ENST00000465573.1:n.376+173A>G (HSPE1)
ENST00000473395.1:n.109A>G (HSPE1)
ENST00000495200.1:n.499A>G (HSPE1)
ENST00000604458.1:c.21A>G (HSPE1-MOB4)	ENSP00000474534.1:p.Arg7=
NM_001202485.1:c.21A>G (HSPE1-MOB4)	NP_001189414.1:p.Arg7=
NM_002157.2:c.21A>G (HSPE1)	NP_002148.1:p.Arg7=
NM_002157.3:c.21A>G (HSPE1) MANE Select	NP_002148.1:p.Arg7=
NM_001202485.2:c.21A>G (HSPE1-MOB4)	NP_001189414.1:p.Arg7=