Canonical Allele Identifier: CA1879980317

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127815291C= , CM000671.2:g.127815291C=	GRCh38
NC_000009.11:g.130577570C= , CM000671.1:g.130577570C=	GRCh37
NC_000009.10:g.129617391C=	NCBI36
NG_009551.1:g.44478G= , LRG_589:g.44478G=
NG_023245.1:g.17417C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.*391G=	ENSP00000479015.1:n.*391G=
ENST00000373203.9:c.*391G= MANE Select	ENSP00000362299.4:n.*391G=
ENST00000344849.4:c.*626G=	ENSP00000341917.3:n.*626G=
ENST00000373203.8:c.*391G=	ENSP00000362299.4:n.*391G=
ENST00000480266.5:c.*391G=	ENSP00000479015.1:n.*391G=
NM_000118.3:c.*626G= , LRG_589t1:c.*626G=	NP_000109.1:n.*626G=
NM_001114753.2:c.*391G= , LRG_589t2:c.*391G=	NP_001108225.1:n.*391G=
NM_001278138.1:c.*391G=	NP_001265067.1:n.*391G=
NM_001114753.3:c.*391G= MANE Select	NP_001108225.1:n.*391G=
NM_001278138.2:c.*391G=	NP_001265067.1:n.*391G=