Canonical Allele Identifier: CA1879980122

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127815200C= , CM000671.2:g.127815200C=	GRCh38
NC_000009.11:g.130577479C= , CM000671.1:g.130577479C=	GRCh37
NC_000009.10:g.129617300C=	NCBI36
NG_009551.1:g.44569G= , LRG_589:g.44569G=
NG_023245.1:g.17326C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.*482G=	ENSP00000479015.1:n.*482G=
ENST00000373203.9:c.*482G= MANE Select	ENSP00000362299.4:n.*482G=
ENST00000344849.4:c.*717G=	ENSP00000341917.3:n.*717G=
ENST00000373203.8:c.*482G=	ENSP00000362299.4:n.*482G=
ENST00000480266.5:c.*482G=	ENSP00000479015.1:n.*482G=
NM_000118.3:c.*717G= , LRG_589t1:c.*717G=	NP_000109.1:n.*717G=
NM_001114753.2:c.*482G= , LRG_589t2:c.*482G=	NP_001108225.1:n.*482G=
NM_001278138.1:c.*482G=	NP_001265067.1:n.*482G=
NM_001114753.3:c.*482G= MANE Select	NP_001108225.1:n.*482G=
NM_001278138.2:c.*482G=	NP_001265067.1:n.*482G=