Canonical Allele Identifier: CA374986465

Gene: ENG

Linked Data

• ClinVar Variation Id: 439650
• ClinVar RCV Id: RCV000507915 ; RCV001217385
• dbSNP Id: rs1554810936
• MyVariant Identifiers: chr9:g.130592107C>T (hg19) ; chr9:g.127829828C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127829828C>T , CM000671.2:g.127829828C>T	GRCh38
NC_000009.11:g.130592107C>T , CM000671.1:g.130592107C>T	GRCh37
NC_000009.10:g.129631928C>T	NCBI36
NG_009551.1:g.29941G>A , LRG_589:g.29941G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000480266.6:c.-327-1G>A	ENSP00000479015.1:n.-327-1G>A
ENST00000373203.9:c.220-1G>A MANE Select	ENSP00000362299.4:n.220-1G>A
ENST00000344849.4:c.220-1G>A	ENSP00000341917.3:n.220-1G>A
ENST00000373203.8:c.220-1G>A	ENSP00000362299.4:n.220-1G>A
ENST00000480266.5:c.-327-1G>A	ENSP00000479015.1:n.-327-1G>A
NM_000118.3:c.220-1G>A , LRG_589t1:c.220-1G>A	NP_000109.1:n.220-1G>A
NM_001114753.2:c.220-1G>A , LRG_589t2:c.220-1G>A	NP_001108225.1:n.220-1G>A
NM_001278138.1:c.-327-1G>A	NP_001265067.1:n.-327-1G>A
XR_001746952.2:n.83-2570C>T
NM_001114753.3:c.220-1G>A MANE Select	NP_001108225.1:n.220-1G>A
NM_001278138.2:c.-327-1G>A	NP_001265067.1:n.-327-1G>A