Canonical Allele Identifier: CA374982638

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127824925C>T , CM000671.2:g.127824925C>T	GRCh38
NC_000009.11:g.130587204C>T , CM000671.1:g.130587204C>T	GRCh37
NC_000009.10:g.129627025C>T	NCBI36
NG_009551.1:g.34844G>A , LRG_589:g.34844G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001114753.3:c.866G>A MANE Select	NP_001108225.1:p.Gly289Asp
ENST00000373203.9:c.866G>A MANE Select	ENSP00000362299.4:p.Gly289Asp
NM_000118.3:c.866G>A , LRG_589t1:c.866G>A	NP_000109.1:p.Gly289Asp
NM_001114753.2:c.866G>A , LRG_589t2:c.866G>A	NP_001108225.1:p.Gly289Asp
NM_001278138.1:c.320G>A	NP_001265067.1:p.Gly107Asp
NM_001278138.2:c.320G>A	NP_001265067.1:p.Gly107Asp
ENST00000344849.4:c.866G>A	ENSP00000341917.3:p.Gly289Asp
ENST00000373203.8:c.866G>A	ENSP00000362299.4:p.Gly289Asp
ENST00000480266.5:c.320G>A	ENSP00000479015.1:p.Gly107Asp
ENST00000480266.6:c.320G>A	ENSP00000479015.1:p.Gly107Asp