Canonical Allele Identifier: CA2695211330

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127826683A>T , CM000671.2:g.127826683A>T	GRCh38
NC_000009.11:g.130588962A>T , CM000671.1:g.130588962A>T	GRCh37
NC_000009.10:g.129628783A>T	NCBI36
NG_009551.1:g.33086T>A , LRG_589:g.33086T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001114753.3:c.361-11T>A MANE Select	NP_001108225.1:n.361-11T>A
ENST00000373203.9:c.361-11T>A MANE Select	ENSP00000362299.4:n.361-11T>A
NM_000118.3:c.361-11T>A , LRG_589t1:c.361-11T>A	NP_000109.1:n.361-11T>A
NM_001114753.2:c.361-11T>A , LRG_589t2:c.361-11T>A	NP_001108225.1:n.361-11T>A
NM_001278138.1:c.-186-11T>A	NP_001265067.1:n.-186-11T>A
NM_001278138.2:c.-186-11T>A	NP_001265067.1:n.-186-11T>A
ENST00000344849.4:c.361-11T>A	ENSP00000341917.3:n.361-11T>A
ENST00000373203.8:c.361-11T>A	ENSP00000362299.4:n.361-11T>A
ENST00000462196.1:n.261-11T>A
ENST00000480266.5:c.-186-11T>A	ENSP00000479015.1:n.-186-11T>A
ENST00000480266.6:c.-186-11T>A	ENSP00000479015.1:n.-186-11T>A
XR_001746952.2:n.82+1225A>T