Canonical Allele Identifier: CA374986286
Gene: ENG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127829790T>C , CM000671.2:g.127829790T>C GRCh38
NC_000009.11:g.130592069T>C , CM000671.1:g.130592069T>C GRCh37
NC_000009.10:g.129631890T>C NCBI36
NG_009551.1:g.29979A>G , LRG_589:g.29979A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000480266.6:c.-290A>G ENSP00000479015.1:n.-290A>G
ENST00000373203.9:c.257A>G MANE Select ENSP00000362299.4:p.Lys86Arg
ENST00000344849.4:c.257A>G ENSP00000341917.3:p.Lys86Arg
ENST00000373203.8:c.257A>G ENSP00000362299.4:p.Lys86Arg
ENST00000462196.1:n.15A>G
ENST00000480266.5:c.-290A>G ENSP00000479015.1:n.-290A>G
NM_000118.3:c.257A>G , LRG_589t1:c.257A>G NP_000109.1:p.Lys86Arg
NM_001114753.2:c.257A>G , LRG_589t2:c.257A>G NP_001108225.1:p.Lys86Arg
NM_001278138.1:c.-290A>G NP_001265067.1:n.-290A>G
XR_001746952.2:n.83-2608T>C
NM_001114753.3:c.257A>G MANE Select NP_001108225.1:p.Lys86Arg
NM_001278138.2:c.-290A>G NP_001265067.1:n.-290A>G