Canonical Allele Identifier: CA1879980057

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127815159T= , CM000671.2:g.127815159T=	GRCh38
NC_000009.11:g.130577438T= , CM000671.1:g.130577438T=	GRCh37
NC_000009.10:g.129617259T=	NCBI36
NG_009551.1:g.44610A= , LRG_589:g.44610A=
NG_023245.1:g.17285T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.*523A=	ENSP00000479015.1:n.*523A=
ENST00000373203.9:c.*523A= MANE Select	ENSP00000362299.4:n.*523A=
ENST00000344849.4:c.*758A=	ENSP00000341917.3:n.*758A=
ENST00000373203.8:c.*523A=	ENSP00000362299.4:n.*523A=
ENST00000480266.5:c.*523A=	ENSP00000479015.1:n.*523A=
NM_000118.3:c.*758A= , LRG_589t1:c.*758A=	NP_000109.1:n.*758A=
NM_001114753.2:c.*523A= , LRG_589t2:c.*523A=	NP_001108225.1:n.*523A=
NM_001278138.1:c.*523A=	NP_001265067.1:n.*523A=
NM_001114753.3:c.*523A= MANE Select	NP_001108225.1:n.*523A=
NM_001278138.2:c.*523A=	NP_001265067.1:n.*523A=