Canonical Allele Identifier: CA1879998778

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127854346C= , CM000671.2:g.127854346C=	GRCh38
NC_000009.11:g.130616625C= , CM000671.1:g.130616625C=	GRCh37
NC_000009.10:g.129656446C=	NCBI36
NG_009551.1:g.5423G= , LRG_589:g.5423G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373203.9:c.10G= MANE Select	ENSP00000362299.4:p.Gly4=
ENST00000344849.4:c.10G=	ENSP00000341917.3:p.Gly4=
ENST00000373203.8:c.10G=	ENSP00000362299.4:p.Gly4=
NM_000118.3:c.10G= , LRG_589t1:c.10G=	NP_000109.1:p.Gly4=
NM_001114753.2:c.10G= , LRG_589t2:c.10G=	NP_001108225.1:p.Gly4=
NM_001114753.3:c.10G= MANE Select	NP_001108225.1:p.Gly4=