Canonical Allele Identifier: CA5253161
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 365095
dbSNP Id: rs767907933

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127829726C>A , CM000671.2:g.127829726C>A GRCh38
NC_000009.11:g.130592005C>A , CM000671.1:g.130592005C>A GRCh37
NC_000009.10:g.129631826C>A NCBI36
NG_009551.1:g.30043G>T , LRG_589:g.30043G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000373203.9:c.321G>T MANE Select ENSP00000362299.4:p.Leu107=
ENST00000344849.4:c.321G>T ENSP00000341917.3:p.Leu107=
ENST00000373203.8:c.321G>T ENSP00000362299.4:p.Leu107=
ENST00000462196.1:n.79G>T
ENST00000480266.5:c.-226G>T ENSP00000479015.1:p.=
NM_000118.3:c.321G>T , LRG_589t1:c.321G>T NP_000109.1:p.Leu107=
NM_001114753.2:c.321G>T , LRG_589t2:c.321G>T NP_001108225.1:p.Leu107=
NM_001278138.1:c.-226G>T NP_001265067.1:p.=
XR_001746952.2:n.83-2672C>A
NM_001114753.3:c.321G>T MANE Select NP_001108225.1:p.Leu107=
NM_001278138.2:c.-226G>T NP_001265067.1:p.=