Canonical Allele Identifier: CA1879998666

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127854292T= , CM000671.2:g.127854292T=	GRCh38
NC_000009.11:g.130616571T= , CM000671.1:g.130616571T=	GRCh37
NC_000009.10:g.129656392T=	NCBI36
NG_009551.1:g.5477A= , LRG_589:g.5477A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373203.9:c.64A= MANE Select	ENSP00000362299.4:p.Thr22=
ENST00000344849.4:c.64A=	ENSP00000341917.3:p.Thr22=
ENST00000373203.8:c.64A=	ENSP00000362299.4:p.Thr22=
NM_000118.3:c.64A= , LRG_589t1:c.64A=	NP_000109.1:p.Thr22=
NM_001114753.2:c.64A= , LRG_589t2:c.64A=	NP_001108225.1:p.Thr22=
NM_001114753.3:c.64A= MANE Select	NP_001108225.1:p.Thr22=