Canonical Allele Identifier: CA1879981734

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127815922G= , CM000671.2:g.127815922G=	GRCh38
NC_000009.11:g.130578201G= , CM000671.1:g.130578201G=	GRCh37
NC_000009.10:g.129618022G=	NCBI36
NG_009551.1:g.43847C= , LRG_589:g.43847C=
NG_023245.1:g.18048G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.1306+21C=	ENSP00000479015.1:n.1306+21C=
ENST00000373203.9:c.1852+21C= MANE Select	ENSP00000362299.4:n.1852+21C=
ENST00000344849.4:c.1873C=	ENSP00000341917.3:p.Gln625=
ENST00000373203.8:c.1852+21C=	ENSP00000362299.4:n.1852+21C=
ENST00000480266.5:c.1306+21C=	ENSP00000479015.1:n.1306+21C=
NM_000118.3:c.1873C= , LRG_589t1:c.1873C=	NP_000109.1:p.Gln625=
NM_001114753.2:c.1852+21C= , LRG_589t2:c.1852+21C=	NP_001108225.1:n.1852+21C=
NM_001278138.1:c.1306+21C=	NP_001265067.1:n.1306+21C=
NM_001114753.3:c.1852+21C= MANE Select	NP_001108225.1:n.1852+21C=
NM_001278138.2:c.1306+21C=	NP_001265067.1:n.1306+21C=