Canonical Allele Identifier: CA590939410

Gene: ENG

Linked Data

• ClinVar Variation Id: 1608621
• ClinVar RCV Id: RCV002147569
• dbSNP Id: rs1316539915
• gnomAD v2: 9-130586729-T-C
• gnomAD v4: 9-127824450-T-C
• MyVariant Identifiers: chr9:g.130586729T>C (hg19) ; chr9:g.127824450T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127824450T>C , CM000671.2:g.127824450T>C	GRCh38
NC_000009.11:g.130586729T>C , CM000671.1:g.130586729T>C	GRCh37
NC_000009.10:g.129626550T>C	NCBI36
NG_009551.1:g.35319A>G , LRG_589:g.35319A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.446-4A>G	ENSP00000479015.1:n.446-4A>G
ENST00000373203.9:c.992-4A>G MANE Select	ENSP00000362299.4:n.992-4A>G
ENST00000344849.4:c.992-4A>G	ENSP00000341917.3:n.992-4A>G
ENST00000373203.8:c.992-4A>G	ENSP00000362299.4:n.992-4A>G
ENST00000480266.5:c.446-4A>G	ENSP00000479015.1:n.446-4A>G
NM_000118.3:c.992-4A>G , LRG_589t1:c.992-4A>G	NP_000109.1:n.992-4A>G
NM_001114753.2:c.992-4A>G , LRG_589t2:c.992-4A>G	NP_001108225.1:n.992-4A>G
NM_001278138.1:c.446-4A>G	NP_001265067.1:n.446-4A>G
NM_001114753.3:c.992-4A>G MANE Select	NP_001108225.1:n.992-4A>G
NM_001278138.2:c.446-4A>G	NP_001265067.1:n.446-4A>G