Canonical Allele Identifier: CA374981732
Gene: ENG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127824423C>A , CM000671.2:g.127824423C>A GRCh38
NC_000009.11:g.130586702C>A , CM000671.1:g.130586702C>A GRCh37
NC_000009.10:g.129626523C>A NCBI36
NG_009551.1:g.35346G>T , LRG_589:g.35346G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000480266.6:c.469G>T ENSP00000479015.1:p.Ala157Ser
ENST00000373203.9:c.1015G>T MANE Select ENSP00000362299.4:p.Ala339Ser
ENST00000344849.4:c.1015G>T ENSP00000341917.3:p.Ala339Ser
ENST00000373203.8:c.1015G>T ENSP00000362299.4:p.Ala339Ser
ENST00000480266.5:c.469G>T ENSP00000479015.1:p.Ala157Ser
NM_000118.3:c.1015G>T , LRG_589t1:c.1015G>T NP_000109.1:p.Ala339Ser
NM_001114753.2:c.1015G>T , LRG_589t2:c.1015G>T NP_001108225.1:p.Ala339Ser
NM_001278138.1:c.469G>T NP_001265067.1:p.Ala157Ser
NM_001114753.3:c.1015G>T MANE Select NP_001108225.1:p.Ala339Ser
NM_001278138.2:c.469G>T NP_001265067.1:p.Ala157Ser