Canonical Allele Identifier: CA1879981377

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127815776G= , CM000671.2:g.127815776G=	GRCh38
NC_000009.11:g.130578055G= , CM000671.1:g.130578055G=	GRCh37
NC_000009.10:g.129617876G=	NCBI36
NG_009551.1:g.43993C= , LRG_589:g.43993C=
NG_023245.1:g.17902G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.1337C=	ENSP00000479015.1:p.Ala446=
ENST00000373203.9:c.1883C= MANE Select	ENSP00000362299.4:p.Ala628=
ENST00000344849.4:c.*141C=	ENSP00000341917.3:n.*141C=
ENST00000373203.8:c.1883C=	ENSP00000362299.4:p.Ala628=
ENST00000480266.5:c.1337C=	ENSP00000479015.1:p.Ala446=
NM_000118.3:c.*141C= , LRG_589t1:c.*141C=	NP_000109.1:n.*141C=
NM_001114753.2:c.1883C= , LRG_589t2:c.1883C=	NP_001108225.1:p.Ala628=
NM_001278138.1:c.1337C=	NP_001265067.1:p.Ala446=
NM_001114753.3:c.1883C= MANE Select	NP_001108225.1:p.Ala628=
NM_001278138.2:c.1337C=	NP_001265067.1:p.Ala446=