Canonical Allele Identifier: CA1879982055

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127816082C= , CM000671.2:g.127816082C=	GRCh38
NC_000009.11:g.130578361C= , CM000671.1:g.130578361C=	GRCh37
NC_000009.10:g.129618182C=	NCBI36
NG_009551.1:g.43687G= , LRG_589:g.43687G=
NG_023245.1:g.18208C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.1196-29G=	ENSP00000479015.1:n.1196-29G=
ENST00000373203.9:c.1742-29G= MANE Select	ENSP00000362299.4:n.1742-29G=
ENST00000344849.4:c.1742-29G=	ENSP00000341917.3:n.1742-29G=
ENST00000373203.8:c.1742-29G=	ENSP00000362299.4:n.1742-29G=
ENST00000480266.5:c.1196-29G=	ENSP00000479015.1:n.1196-29G=
NM_000118.3:c.1742-29G= , LRG_589t1:c.1742-29G=	NP_000109.1:n.1742-29G=
NM_001114753.2:c.1742-29G= , LRG_589t2:c.1742-29G=	NP_001108225.1:n.1742-29G=
NM_001278138.1:c.1196-29G=	NP_001265067.1:n.1196-29G=
XM_011519273.1:c.-497C=	XP_011517575.1:n.-497C=
NR_136302.1:n.17C=
NM_001114753.3:c.1742-29G= MANE Select	NP_001108225.1:n.1742-29G=
NM_001278138.2:c.1196-29G=	NP_001265067.1:n.1196-29G=