Canonical Allele Identifier: CA2662516833

Gene: HSPE1 HSPD1 HSPE1-MOB4

Linked Data

• gnomAD v4: 2-197500967-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.197500967G>A , CM000664.2:g.197500967G>A	GRCh38
NC_000002.11:g.198365691G>A , CM000664.1:g.198365691G>A	GRCh37
NC_000002.10:g.198073936G>A	NCBI36
NG_008914.1:g.5971G>A
NG_008915.1:g.4308C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000233893.10:c.4-107G>A (HSPE1) MANE Select	ENSP00000233893.5:n.4-107G>A
ENST00000426480.2:c.-2-2117C>T (HSPD1)	ENSP00000414446.2:n.-2-2117C>T
ENST00000233893.9:c.4-107G>A (HSPE1)	ENSP00000233893.5:n.4-107G>A
ENST00000409468.1:c.4-107G>A (HSPE1)	ENSP00000386447.1:n.4-107G>A
ENST00000409729.1:c.3+528G>A (HSPE1)	ENSP00000387101.1:n.3+528G>A
ENST00000426480.1:c.125-2117C>T (HSPD1)	ENSP00000414446.1:n.125-2117C>T
ENST00000463841.1:n.86G>A (HSPE1)
ENST00000465573.1:n.376+49G>A (HSPE1)
ENST00000473395.1:n.92-107G>A (HSPE1)
ENST00000495200.1:n.481+49G>A (HSPE1)
ENST00000604458.1:c.4-107G>A (HSPE1-MOB4)	ENSP00000474534.1:n.4-107G>A
NM_001202485.1:c.4-107G>A (HSPE1-MOB4)	NP_001189414.1:n.4-107G>A
NM_002157.2:c.4-107G>A (HSPE1)	NP_002148.1:n.4-107G>A
NM_002157.3:c.4-107G>A (HSPE1) MANE Select	NP_002148.1:n.4-107G>A
NM_001202485.2:c.4-107G>A (HSPE1-MOB4)	NP_001189414.1:n.4-107G>A