Canonical Allele Identifier: CA2840996448

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127826440G>C , CM000671.2:g.127826440G>C	GRCh38
NC_000009.11:g.130588719G>C , CM000671.1:g.130588719G>C	GRCh37
NC_000009.10:g.129628540G>C	NCBI36
NG_009551.1:g.33329C>G , LRG_589:g.33329C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.-24+70C>G	ENSP00000479015.1:n.-24+70C>G
ENST00000373203.9:c.523+70C>G MANE Select	ENSP00000362299.4:n.523+70C>G
ENST00000344849.4:c.523+70C>G	ENSP00000341917.3:n.523+70C>G
ENST00000373203.8:c.523+70C>G	ENSP00000362299.4:n.523+70C>G
ENST00000462196.1:n.423+70C>G
ENST00000480266.5:c.-24+70C>G	ENSP00000479015.1:n.-24+70C>G
NM_000118.3:c.523+70C>G , LRG_589t1:c.523+70C>G	NP_000109.1:n.523+70C>G
NM_001114753.2:c.523+70C>G , LRG_589t2:c.523+70C>G	NP_001108225.1:n.523+70C>G
NM_001278138.1:c.-24+70C>G	NP_001265067.1:n.-24+70C>G
XR_001746952.2:n.82+982G>C
NM_001114753.3:c.523+70C>G MANE Select	NP_001108225.1:n.523+70C>G
NM_001278138.2:c.-24+70C>G	NP_001265067.1:n.-24+70C>G