Canonical Allele Identifier: CA1879987230

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127818745T= , CM000671.2:g.127818745T=	GRCh38
NC_000009.11:g.130581024T= , CM000671.1:g.130581024T=	GRCh37
NC_000009.10:g.129620845T=	NCBI36
NG_009551.1:g.41024A= , LRG_589:g.41024A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000480266.6:c.853A=	ENSP00000479015.1:p.Ile285=
ENST00000373203.9:c.1399A= MANE Select	ENSP00000362299.4:p.Ile467=
ENST00000344849.4:c.1399A=	ENSP00000341917.3:p.Ile467=
ENST00000373203.8:c.1399A=	ENSP00000362299.4:p.Ile467=
ENST00000480266.5:c.853A=	ENSP00000479015.1:p.Ile285=
NM_000118.3:c.1399A= , LRG_589t1:c.1399A=	NP_000109.1:p.Ile467=
NM_001114753.2:c.1399A= , LRG_589t2:c.1399A=	NP_001108225.1:p.Ile467=
NM_001278138.1:c.853A=	NP_001265067.1:p.Ile285=
NR_136302.1:n.1568+34T=
NM_001114753.3:c.1399A= MANE Select	NP_001108225.1:p.Ile467=
NM_001278138.2:c.853A=	NP_001265067.1:p.Ile285=