Canonical Allele Identifier: CA860193647
Gene: ENG HGNC NCBI

Linked Data

dbSNP Id: rs1195961078

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127819543C>T , CM000671.2:g.127819543C>T GRCh38
NC_000009.11:g.130581822C>T , CM000671.1:g.130581822C>T GRCh37
NC_000009.10:g.129621643C>T NCBI36
NG_009551.1:g.40226G>A , LRG_589:g.40226G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000480266.6:c.765+79G>A ENSP00000479015.1:n.765+79G>A
ENST00000373203.9:c.1311+79G>A MANE Select ENSP00000362299.4:n.1311+79G>A
ENST00000344849.4:c.1311+79G>A ENSP00000341917.3:n.1311+79G>A
ENST00000373203.8:c.1311+79G>A ENSP00000362299.4:n.1311+79G>A
ENST00000480266.5:c.765+79G>A ENSP00000479015.1:n.765+79G>A
ENST00000486329.1:n.358G>A
NM_000118.3:c.1311+79G>A , LRG_589t1:c.1311+79G>A NP_000109.1:n.1311+79G>A
NM_001114753.2:c.1311+79G>A , LRG_589t2:c.1311+79G>A NP_001108225.1:n.1311+79G>A
NM_001278138.1:c.765+79G>A NP_001265067.1:n.765+79G>A
NR_136302.1:n.1568+832C>T
NM_001114753.3:c.1311+79G>A MANE Select NP_001108225.1:n.1311+79G>A
NM_001278138.2:c.765+79G>A NP_001265067.1:n.765+79G>A