Canonical Allele Identifier: CA2579461239

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127815862A>C , CM000671.2:g.127815862A>C	GRCh38
NC_000009.11:g.130578141A>C , CM000671.1:g.130578141A>C	GRCh37
NC_000009.10:g.129617962A>C	NCBI36
NG_009551.1:g.43907T>G , LRG_589:g.43907T>G
NG_023245.1:g.17988A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.1307-56T>G	ENSP00000479015.1:n.1307-56T>G
ENST00000373203.9:c.1853-56T>G MANE Select	ENSP00000362299.4:n.1853-56T>G
ENST00000344849.4:c.*55T>G	ENSP00000341917.3:n.*55T>G
ENST00000373203.8:c.1853-56T>G	ENSP00000362299.4:n.1853-56T>G
ENST00000480266.5:c.1307-56T>G	ENSP00000479015.1:n.1307-56T>G
NM_000118.3:c.*55T>G , LRG_589t1:c.*55T>G	NP_000109.1:n.*55T>G
NM_001114753.2:c.1853-56T>G , LRG_589t2:c.1853-56T>G	NP_001108225.1:n.1853-56T>G
NM_001278138.1:c.1307-56T>G	NP_001265067.1:n.1307-56T>G
NM_001114753.3:c.1853-56T>G MANE Select	NP_001108225.1:n.1853-56T>G
NM_001278138.2:c.1307-56T>G	NP_001265067.1:n.1307-56T>G