Canonical Allele Identifier: CA2691810608
Gene: ENG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127854380C>A , CM000671.2:g.127854380C>A GRCh38
NC_000009.11:g.130616659C>A , CM000671.1:g.130616659C>A GRCh37
NC_000009.10:g.129656480C>A NCBI36
NG_009551.1:g.5389G>T , LRG_589:g.5389G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373203.9:c.-25G>T MANE Select ENSP00000362299.4:n.-25G>T
ENST00000344849.4:c.-25G>T ENSP00000341917.3:n.-25G>T
ENST00000373203.8:c.-25G>T ENSP00000362299.4:n.-25G>T
NM_000118.3:c.-25G>T , LRG_589t1:c.-25G>T NP_000109.1:n.-25G>T
NM_001114753.2:c.-25G>T , LRG_589t2:c.-25G>T NP_001108225.1:n.-25G>T
NM_001114753.3:c.-25G>T MANE Select NP_001108225.1:n.-25G>T