Canonical Allele Identifier: CA1879982029

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127816067A= , CM000671.2:g.127816067A=	GRCh38
NC_000009.11:g.130578346A= , CM000671.1:g.130578346A=	GRCh37
NC_000009.10:g.129618167A=	NCBI36
NG_009551.1:g.43702T= , LRG_589:g.43702T=
NG_023245.1:g.18193A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.1196-14T=	ENSP00000479015.1:n.1196-14T=
ENST00000373203.9:c.1742-14T= MANE Select	ENSP00000362299.4:n.1742-14T=
ENST00000344849.4:c.1742-14T=	ENSP00000341917.3:n.1742-14T=
ENST00000373203.8:c.1742-14T=	ENSP00000362299.4:n.1742-14T=
ENST00000480266.5:c.1196-14T=	ENSP00000479015.1:n.1196-14T=
NM_000118.3:c.1742-14T= , LRG_589t1:c.1742-14T=	NP_000109.1:n.1742-14T=
NM_001114753.2:c.1742-14T= , LRG_589t2:c.1742-14T=	NP_001108225.1:n.1742-14T=
NM_001278138.1:c.1196-14T=	NP_001265067.1:n.1196-14T=
XM_011519273.1:c.-512A=	XP_011517575.1:n.-512A=
NR_136302.1:n.2A=
NM_001114753.3:c.1742-14T= MANE Select	NP_001108225.1:n.1742-14T=
NM_001278138.2:c.1196-14T=	NP_001265067.1:n.1196-14T=