Canonical Allele Identifier: CA1879989829

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127819964A= , CM000671.2:g.127819964A=	GRCh38
NC_000009.11:g.130582243A= , CM000671.1:g.130582243A=	GRCh37
NC_000009.10:g.129622064A=	NCBI36
NG_009551.1:g.39805T= , LRG_589:g.39805T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.662T=	ENSP00000479015.1:p.Phe221=
ENST00000373203.9:c.1208T= MANE Select	ENSP00000362299.4:p.Phe403=
ENST00000344849.4:c.1208T=	ENSP00000341917.3:p.Phe403=
ENST00000373203.8:c.1208T=	ENSP00000362299.4:p.Phe403=
ENST00000480266.5:c.662T=	ENSP00000479015.1:p.Phe221=
ENST00000486329.1:n.176T=
NM_000118.3:c.1208T= , LRG_589t1:c.1208T=	NP_000109.1:p.Phe403=
NM_001114753.2:c.1208T= , LRG_589t2:c.1208T=	NP_001108225.1:p.Phe403=
NM_001278138.1:c.662T=	NP_001265067.1:p.Phe221=
NR_136302.1:n.1569-1231A=
NM_001114753.3:c.1208T= MANE Select	NP_001108225.1:p.Phe403=
NM_001278138.2:c.662T=	NP_001265067.1:p.Phe221=