Canonical Allele Identifier: CA1879981307

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127815754C= , CM000671.2:g.127815754C=	GRCh38
NC_000009.11:g.130578033C= , CM000671.1:g.130578033C=	GRCh37
NC_000009.10:g.129617854C=	NCBI36
NG_009551.1:g.44015G= , LRG_589:g.44015G=
NG_023245.1:g.17880C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.1359G=	ENSP00000479015.1:p.Ser453=
ENST00000373203.9:c.1905G= MANE Select	ENSP00000362299.4:p.Ser635=
ENST00000344849.4:c.*163G=	ENSP00000341917.3:n.*163G=
ENST00000373203.8:c.1905G=	ENSP00000362299.4:p.Ser635=
ENST00000480266.5:c.1359G=	ENSP00000479015.1:p.Ser453=
NM_000118.3:c.*163G= , LRG_589t1:c.*163G=	NP_000109.1:n.*163G=
NM_001114753.2:c.1905G= , LRG_589t2:c.1905G=	NP_001108225.1:p.Ser635=
NM_001278138.1:c.1359G=	NP_001265067.1:p.Ser453=
NM_001114753.3:c.1905G= MANE Select	NP_001108225.1:p.Ser635=
NM_001278138.2:c.1359G=	NP_001265067.1:p.Ser453=