Canonical Allele Identifier: CA1879981853

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127829741G= , CM000671.2:g.127829741G=	GRCh38
NC_000009.11:g.130592020G= , CM000671.1:g.130592020G=	GRCh37
NC_000009.10:g.129631841G=	NCBI36
NG_009551.1:g.30028C= , LRG_589:g.30028C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.-241C=	ENSP00000479015.1:n.-241C=
ENST00000373203.9:c.306C= MANE Select	ENSP00000362299.4:p.Asn102=
ENST00000344849.4:c.306C=	ENSP00000341917.3:p.Asn102=
ENST00000373203.8:c.306C=	ENSP00000362299.4:p.Asn102=
ENST00000462196.1:n.64C=
ENST00000480266.5:c.-241C=	ENSP00000479015.1:n.-241C=
NM_000118.3:c.306C= , LRG_589t1:c.306C=	NP_000109.1:p.Asn102=
NM_001114753.2:c.306C= , LRG_589t2:c.306C=	NP_001108225.1:p.Asn102=
NM_001278138.1:c.-241C=	NP_001265067.1:n.-241C=
XR_001746952.2:n.83-2657G=
NM_001114753.3:c.306C= MANE Select	NP_001108225.1:p.Asn102=
NM_001278138.2:c.-241C=	NP_001265067.1:n.-241C=