Canonical Allele Identifier: CA1879976473

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127825862T= , CM000671.2:g.127825862T=	GRCh38
NC_000009.11:g.130588141T= , CM000671.1:g.130588141T=	GRCh37
NC_000009.10:g.129627962T=	NCBI36
NG_009551.1:g.33907A= , LRG_589:g.33907A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.-23-2A=	ENSP00000479015.1:n.-23-2A=
ENST00000373203.9:c.524-2A= MANE Select	ENSP00000362299.4:n.524-2A=
ENST00000344849.4:c.524-2A=	ENSP00000341917.3:n.524-2A=
ENST00000373203.8:c.524-2A=	ENSP00000362299.4:n.524-2A=
ENST00000462196.1:n.424-2A=
ENST00000480266.5:c.-23-2A=	ENSP00000479015.1:n.-23-2A=
NM_000118.3:c.524-2A= , LRG_589t1:c.524-2A=	NP_000109.1:n.524-2A=
NM_001114753.2:c.524-2A= , LRG_589t2:c.524-2A=	NP_001108225.1:n.524-2A=
NM_001278138.1:c.-23-2A=	NP_001265067.1:n.-23-2A=
XR_001746952.2:n.82+404T=
NM_001114753.3:c.524-2A= MANE Select	NP_001108225.1:n.524-2A=
NM_001278138.2:c.-23-2A=	NP_001265067.1:n.-23-2A=