Canonical Allele Identifier: CA374984245

Gene: ENG

Linked Data

• MyVariant Identifiers: chr9:g.130588861C>T (hg19) ; chr9:g.127826582C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127826582C>T , CM000671.2:g.127826582C>T	GRCh38
NC_000009.11:g.130588861C>T , CM000671.1:g.130588861C>T	GRCh37
NC_000009.10:g.129628682C>T	NCBI36
NG_009551.1:g.33187G>A , LRG_589:g.33187G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.-96G>A	ENSP00000479015.1:n.-96G>A
ENST00000373203.9:c.451G>A MANE Select	ENSP00000362299.4:p.Ala151Thr
ENST00000344849.4:c.451G>A	ENSP00000341917.3:p.Ala151Thr
ENST00000373203.8:c.451G>A	ENSP00000362299.4:p.Ala151Thr
ENST00000462196.1:n.351G>A
ENST00000480266.5:c.-96G>A	ENSP00000479015.1:n.-96G>A
NM_000118.3:c.451G>A , LRG_589t1:c.451G>A	NP_000109.1:p.Ala151Thr
NM_001114753.2:c.451G>A , LRG_589t2:c.451G>A	NP_001108225.1:p.Ala151Thr
NM_001278138.1:c.-96G>A	NP_001265067.1:n.-96G>A
XR_001746952.2:n.82+1124C>T
NM_001114753.3:c.451G>A MANE Select	NP_001108225.1:p.Ala151Thr
NM_001278138.2:c.-96G>A	NP_001265067.1:n.-96G>A