Canonical Allele Identifier: CA374984493

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127826674T>A , CM000671.2:g.127826674T>A	GRCh38
NC_000009.11:g.130588953T>A , CM000671.1:g.130588953T>A	GRCh37
NC_000009.10:g.129628774T>A	NCBI36
NG_009551.1:g.33095A>T , LRG_589:g.33095A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001114753.3:c.361-2A>T MANE Select	NP_001108225.1:n.361-2A>T
ENST00000373203.9:c.361-2A>T MANE Select	ENSP00000362299.4:n.361-2A>T
NM_000118.3:c.361-2A>T , LRG_589t1:c.361-2A>T	NP_000109.1:n.361-2A>T
NM_001114753.2:c.361-2A>T , LRG_589t2:c.361-2A>T	NP_001108225.1:n.361-2A>T
NM_001278138.1:c.-186-2A>T	NP_001265067.1:n.-186-2A>T
NM_001278138.2:c.-186-2A>T	NP_001265067.1:n.-186-2A>T
ENST00000344849.4:c.361-2A>T	ENSP00000341917.3:n.361-2A>T
ENST00000373203.8:c.361-2A>T	ENSP00000362299.4:n.361-2A>T
ENST00000462196.1:n.261-2A>T
ENST00000480266.5:c.-186-2A>T	ENSP00000479015.1:n.-186-2A>T
ENST00000480266.6:c.-186-2A>T	ENSP00000479015.1:n.-186-2A>T
XR_001746952.2:n.82+1216T>A