Canonical Allele Identifier: CA1879982073

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127816088T= , CM000671.2:g.127816088T=	GRCh38
NC_000009.11:g.130578367T= , CM000671.1:g.130578367T=	GRCh37
NC_000009.10:g.129618188T=	NCBI36
NG_009551.1:g.43681A= , LRG_589:g.43681A=
NG_023245.1:g.18214T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.1196-35A=	ENSP00000479015.1:n.1196-35A=
ENST00000373203.9:c.1742-35A= MANE Select	ENSP00000362299.4:n.1742-35A=
ENST00000344849.4:c.1742-35A=	ENSP00000341917.3:n.1742-35A=
ENST00000373203.8:c.1742-35A=	ENSP00000362299.4:n.1742-35A=
ENST00000480266.5:c.1196-35A=	ENSP00000479015.1:n.1196-35A=
NM_000118.3:c.1742-35A= , LRG_589t1:c.1742-35A=	NP_000109.1:n.1742-35A=
NM_001114753.2:c.1742-35A= , LRG_589t2:c.1742-35A=	NP_001108225.1:n.1742-35A=
NM_001278138.1:c.1196-35A=	NP_001265067.1:n.1196-35A=
XM_011519273.1:c.-491T=	XP_011517575.1:n.-491T=
NR_136302.1:n.23T=
NM_001114753.3:c.1742-35A= MANE Select	NP_001108225.1:n.1742-35A=
NM_001278138.2:c.1196-35A=	NP_001265067.1:n.1196-35A=