Canonical Allele Identifier: CA374977872

Gene: ENG

Linked Data

• ClinVar Variation Id: 453196
• ClinVar RCV Id: RCV000523118 ; RCV001219462 ; RCV002384020
• dbSNP Id: rs1554809361
• MyVariant Identifiers: chr9:g.130581097G>T (hg19) ; chr9:g.127818818G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127818818G>T , CM000671.2:g.127818818G>T	GRCh38
NC_000009.11:g.130581097G>T , CM000671.1:g.130581097G>T	GRCh37
NC_000009.10:g.129620918G>T	NCBI36
NG_009551.1:g.40951C>A , LRG_589:g.40951C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.780C>A	ENSP00000479015.1:p.Cys260Ter
ENST00000373203.9:c.1326C>A MANE Select	ENSP00000362299.4:p.Cys442Ter
ENST00000344849.4:c.1326C>A	ENSP00000341917.3:p.Cys442Ter
ENST00000373203.8:c.1326C>A	ENSP00000362299.4:p.Cys442Ter
ENST00000480266.5:c.780C>A	ENSP00000479015.1:p.Cys260Ter
NM_000118.3:c.1326C>A , LRG_589t1:c.1326C>A	NP_000109.1:p.Cys442Ter
NM_001114753.2:c.1326C>A , LRG_589t2:c.1326C>A	NP_001108225.1:p.Cys442Ter
NM_001278138.1:c.780C>A	NP_001265067.1:p.Cys260Ter
NR_136302.1:n.1568+107G>T
NM_001114753.3:c.1326C>A MANE Select	NP_001108225.1:p.Cys442Ter
NM_001278138.2:c.780C>A	NP_001265067.1:p.Cys260Ter