Canonical Allele Identifier: CA1879981999

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127816047G= , CM000671.2:g.127816047G=	GRCh38
NC_000009.11:g.130578326G= , CM000671.1:g.130578326G=	GRCh37
NC_000009.10:g.129618147G=	NCBI36
NG_009551.1:g.43722C= , LRG_589:g.43722C=
NG_023245.1:g.18173G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.1202C=	ENSP00000479015.1:p.Thr401=
ENST00000373203.9:c.1748C= MANE Select	ENSP00000362299.4:p.Thr583=
ENST00000344849.4:c.1748C=	ENSP00000341917.3:p.Thr583=
ENST00000373203.8:c.1748C=	ENSP00000362299.4:p.Thr583=
ENST00000480266.5:c.1202C=	ENSP00000479015.1:p.Thr401=
NM_000118.3:c.1748C= , LRG_589t1:c.1748C=	NP_000109.1:p.Thr583=
NM_001114753.2:c.1748C= , LRG_589t2:c.1748C=	NP_001108225.1:p.Thr583=
NM_001278138.1:c.1202C=	NP_001265067.1:p.Thr401=
NM_001114753.3:c.1748C= MANE Select	NP_001108225.1:p.Thr583=
NM_001278138.2:c.1202C=	NP_001265067.1:p.Thr401=