Canonical Allele Identifier: CA2691810607
Gene: ENG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127854379G>T , CM000671.2:g.127854379G>T GRCh38
NC_000009.11:g.130616658G>T , CM000671.1:g.130616658G>T GRCh37
NC_000009.10:g.129656479G>T NCBI36
NG_009551.1:g.5390C>A , LRG_589:g.5390C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373203.9:c.-24C>A MANE Select ENSP00000362299.4:n.-24C>A
ENST00000344849.4:c.-24C>A ENSP00000341917.3:n.-24C>A
ENST00000373203.8:c.-24C>A ENSP00000362299.4:n.-24C>A
NM_000118.3:c.-24C>A , LRG_589t1:c.-24C>A NP_000109.1:n.-24C>A
NM_001114753.2:c.-24C>A , LRG_589t2:c.-24C>A NP_001108225.1:n.-24C>A
NM_001114753.3:c.-24C>A MANE Select NP_001108225.1:n.-24C>A