Canonical Allele Identifier: CA374983805

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127825858G>A , CM000671.2:g.127825858G>A	GRCh38
NC_000009.11:g.130588137G>A , CM000671.1:g.130588137G>A	GRCh37
NC_000009.10:g.129627958G>A	NCBI36
NG_009551.1:g.33911C>T , LRG_589:g.33911C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001114753.3:c.526C>T MANE Select	NP_001108225.1:p.Gln176Ter
ENST00000373203.9:c.526C>T MANE Select	ENSP00000362299.4:p.Gln176Ter
NM_000118.3:c.526C>T , LRG_589t1:c.526C>T	NP_000109.1:p.Gln176Ter
NM_001114753.2:c.526C>T , LRG_589t2:c.526C>T	NP_001108225.1:p.Gln176Ter
NM_001278138.1:c.-21C>T	NP_001265067.1:n.-21C>T
NM_001278138.2:c.-21C>T	NP_001265067.1:n.-21C>T
ENST00000344849.4:c.526C>T	ENSP00000341917.3:p.Gln176Ter
ENST00000373203.8:c.526C>T	ENSP00000362299.4:p.Gln176Ter
ENST00000462196.1:n.426C>T
ENST00000480266.5:c.-21C>T	ENSP00000479015.1:n.-21C>T
ENST00000480266.6:c.-21C>T	ENSP00000479015.1:n.-21C>T
XR_001746952.2:n.82+400G>A