Canonical Allele Identifier: CA2662516703
Gene: HSPE1 HGNC NCBI
HSPD1 HGNC NCBI
HSPE1-MOB4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.197500818A>G , CM000664.2:g.197500818A>G GRCh38
NC_000002.11:g.198365542A>G , CM000664.1:g.198365542A>G GRCh37
NC_000002.10:g.198073787A>G NCBI36
NG_008914.1:g.5822A>G
NG_008915.1:g.4457T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000233893.10:c.4-256A>G (HSPE1) MANE Select ENSP00000233893.5:n.4-256A>G
ENST00000426480.2:c.-2-1968T>C (HSPD1) ENSP00000414446.2:n.-2-1968T>C
ENST00000233893.9:c.4-256A>G (HSPE1) ENSP00000233893.5:n.4-256A>G
ENST00000409468.1:c.4-256A>G (HSPE1) ENSP00000386447.1:n.4-256A>G
ENST00000409729.1:c.3+379A>G (HSPE1) ENSP00000387101.1:n.3+379A>G
ENST00000426480.1:c.125-1968T>C (HSPD1) ENSP00000414446.1:n.125-1968T>C
ENST00000465573.1:n.276A>G (HSPE1)
ENST00000473395.1:n.92-256A>G (HSPE1)
ENST00000495200.1:n.381A>G (HSPE1)
ENST00000604458.1:c.4-256A>G (HSPE1-MOB4) ENSP00000474534.1:n.4-256A>G
NM_001202485.1:c.4-256A>G (HSPE1-MOB4) NP_001189414.1:n.4-256A>G
NM_002157.2:c.4-256A>G (HSPE1) NP_002148.1:n.4-256A>G
NM_002157.3:c.4-256A>G (HSPE1) MANE Select NP_002148.1:n.4-256A>G
NM_001202485.2:c.4-256A>G (HSPE1-MOB4) NP_001189414.1:n.4-256A>G