Canonical Allele Identifier: CA1879980151

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127815215G= , CM000671.2:g.127815215G=	GRCh38
NC_000009.11:g.130577494G= , CM000671.1:g.130577494G=	GRCh37
NC_000009.10:g.129617315G=	NCBI36
NG_009551.1:g.44554C= , LRG_589:g.44554C=
NG_023245.1:g.17341G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.*467C=	ENSP00000479015.1:n.*467C=
ENST00000373203.9:c.*467C= MANE Select	ENSP00000362299.4:n.*467C=
ENST00000344849.4:c.*702C=	ENSP00000341917.3:n.*702C=
ENST00000373203.8:c.*467C=	ENSP00000362299.4:n.*467C=
ENST00000480266.5:c.*467C=	ENSP00000479015.1:n.*467C=
NM_000118.3:c.*702C= , LRG_589t1:c.*702C=	NP_000109.1:n.*702C=
NM_001114753.2:c.*467C= , LRG_589t2:c.*467C=	NP_001108225.1:n.*467C=
NM_001278138.1:c.*467C=	NP_001265067.1:n.*467C=
NM_001114753.3:c.*467C= MANE Select	NP_001108225.1:n.*467C=
NM_001278138.2:c.*467C=	NP_001265067.1:n.*467C=