Canonical Allele Identifier: CA2662516672

Gene: HSPE1 HSPD1 HSPE1-MOB4

Linked Data

• gnomAD v4: 2-197500781-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.197500781T>C , CM000664.2:g.197500781T>C	GRCh38
NC_000002.11:g.198365505T>C , CM000664.1:g.198365505T>C	GRCh37
NC_000002.10:g.198073750T>C	NCBI36
NG_008914.1:g.5785T>C
NG_008915.1:g.4494A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233893.10:c.4-293T>C (HSPE1) MANE Select	ENSP00000233893.5:n.4-293T>C
ENST00000426480.2:c.-2-1931A>G (HSPD1)	ENSP00000414446.2:n.-2-1931A>G
ENST00000233893.9:c.4-293T>C (HSPE1)	ENSP00000233893.5:n.4-293T>C
ENST00000409468.1:c.4-293T>C (HSPE1)	ENSP00000386447.1:n.4-293T>C
ENST00000409729.1:c.3+342T>C (HSPE1)	ENSP00000387101.1:n.3+342T>C
ENST00000426480.1:c.125-1931A>G (HSPD1)	ENSP00000414446.1:n.125-1931A>G
ENST00000465573.1:n.239T>C (HSPE1)
ENST00000473395.1:n.92-293T>C (HSPE1)
ENST00000495200.1:n.344T>C (HSPE1)
ENST00000604458.1:c.4-293T>C (HSPE1-MOB4)	ENSP00000474534.1:n.4-293T>C
NM_001202485.1:c.4-293T>C (HSPE1-MOB4)	NP_001189414.1:n.4-293T>C
NM_002157.2:c.4-293T>C (HSPE1)	NP_002148.1:n.4-293T>C
NM_002157.3:c.4-293T>C (HSPE1) MANE Select	NP_002148.1:n.4-293T>C
NM_001202485.2:c.4-293T>C (HSPE1-MOB4)	NP_001189414.1:n.4-293T>C