Canonical Allele Identifier: CA5252675

Gene: ENG

Linked Data

• ClinVar Variation Id: 407125
• ClinVar RCV Id: RCV002261089 ; RCV003153610
• dbSNP Id: rs781201877
• ExAC: 9:130579467 C / T
• gnomAD v2: 9-130579467-C-T
• gnomAD v3: 9-127817188-C-T
• gnomAD v4: 9-127817188-C-T
• MyVariant Identifiers: chr9:g.130579467C>T (hg19) ; chr9:g.127817188C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127817188C>T , CM000671.2:g.127817188C>T	GRCh38
NC_000009.11:g.130579467C>T , CM000671.1:g.130579467C>T	GRCh37
NC_000009.10:g.129619288C>T	NCBI36
NG_009551.1:g.42581G>A , LRG_589:g.42581G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.1156G>A	ENSP00000479015.1:p.Val386Ile
ENST00000373203.9:c.1702G>A MANE Select	ENSP00000362299.4:p.Val568Ile
ENST00000344849.4:c.1702G>A	ENSP00000341917.3:p.Val568Ile
ENST00000373203.8:c.1702G>A	ENSP00000362299.4:p.Val568Ile
ENST00000480266.5:c.1156G>A	ENSP00000479015.1:p.Val386Ile
NM_000118.3:c.1702G>A , LRG_589t1:c.1702G>A	NP_000109.1:p.Val568Ile
NM_001114753.2:c.1702G>A , LRG_589t2:c.1702G>A	NP_001108225.1:p.Val568Ile
NM_001278138.1:c.1156G>A	NP_001265067.1:p.Val386Ile
NR_136302.1:n.1123C>T
NM_001114753.3:c.1702G>A MANE Select	NP_001108225.1:p.Val568Ile
NM_001278138.2:c.1156G>A	NP_001265067.1:p.Val386Ile