Canonical Allele Identifier: CA374971519

Gene: ENG

Linked Data

• ClinVar Variation Id: 1381531
• ClinVar RCV Id: RCV001895413
• dbSNP Id: rs1346184000
• gnomAD v2: 9-130578222-G-A
• gnomAD v3: 9-127815943-G-A
• gnomAD v4: 9-127815943-G-A
• MyVariant Identifiers: chr9:g.130578222G>A (hg19) ; chr9:g.127815943G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127815943G>A , CM000671.2:g.127815943G>A	GRCh38
NC_000009.11:g.130578222G>A , CM000671.1:g.130578222G>A	GRCh37
NC_000009.10:g.129618043G>A	NCBI36
NG_009551.1:g.43826C>T , LRG_589:g.43826C>T
NG_023245.1:g.18069G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.1306C>T	ENSP00000479015.1:p.Arg436Cys
ENST00000373203.9:c.1852C>T MANE Select	ENSP00000362299.4:p.Arg618Cys
ENST00000344849.4:c.1852C>T	ENSP00000341917.3:p.Arg618Cys
ENST00000373203.8:c.1852C>T	ENSP00000362299.4:p.Arg618Cys
ENST00000480266.5:c.1306C>T	ENSP00000479015.1:p.Arg436Cys
NM_000118.3:c.1852C>T , LRG_589t1:c.1852C>T	NP_000109.1:p.Arg618Cys
NM_001114753.2:c.1852C>T , LRG_589t2:c.1852C>T	NP_001108225.1:p.Arg618Cys
NM_001278138.1:c.1306C>T	NP_001265067.1:p.Arg436Cys
NM_001114753.3:c.1852C>T MANE Select	NP_001108225.1:p.Arg618Cys
NM_001278138.2:c.1306C>T	NP_001265067.1:p.Arg436Cys