Canonical Allele Identifier: CA374983621

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127825764C>T , CM000671.2:g.127825764C>T	GRCh38
NC_000009.11:g.130588043C>T , CM000671.1:g.130588043C>T	GRCh37
NC_000009.10:g.129627864C>T	NCBI36
NG_009551.1:g.34005G>A , LRG_589:g.34005G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001114753.3:c.620G>A MANE Select	NP_001108225.1:p.Cys207Tyr
ENST00000373203.9:c.620G>A MANE Select	ENSP00000362299.4:p.Cys207Tyr
NM_000118.3:c.620G>A , LRG_589t1:c.620G>A	NP_000109.1:p.Cys207Tyr
NM_001114753.2:c.620G>A , LRG_589t2:c.620G>A	NP_001108225.1:p.Cys207Tyr
NM_001278138.1:c.74G>A	NP_001265067.1:p.Cys25Tyr
NM_001278138.2:c.74G>A	NP_001265067.1:p.Cys25Tyr
ENST00000344849.4:c.620G>A	ENSP00000341917.3:p.Cys207Tyr
ENST00000373203.8:c.620G>A	ENSP00000362299.4:p.Cys207Tyr
ENST00000480266.5:c.74G>A	ENSP00000479015.1:p.Cys25Tyr
ENST00000480266.6:c.74G>A	ENSP00000479015.1:p.Cys25Tyr
XR_001746952.2:n.82+306C>T