Canonical Allele Identifier: CA322731

Gene: ENG

Linked Data

• ClinVar Variation Id: 213216
• ClinVar RCV Id: RCV000198224 ; RCV000551278 ; RCV001286561 ; RCV002390514
• dbSNP Id: rs863223542
• MyVariant Identifiers: chr9:g.130580994C>T (hg19) ; chr9:g.127818715C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127818715C>T , CM000671.2:g.127818715C>T	GRCh38
NC_000009.11:g.130580994C>T , CM000671.1:g.130580994C>T	GRCh37
NC_000009.10:g.129620815C>T	NCBI36
NG_009551.1:g.41054G>A , LRG_589:g.41054G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.882+1G>A	ENSP00000479015.1:n.882+1G>A
ENST00000373203.9:c.1428+1G>A MANE Select	ENSP00000362299.4:n.1428+1G>A
ENST00000344849.4:c.1428+1G>A	ENSP00000341917.3:n.1428+1G>A
ENST00000373203.8:c.1428+1G>A	ENSP00000362299.4:n.1428+1G>A
ENST00000480266.5:c.882+1G>A	ENSP00000479015.1:n.882+1G>A
NM_000118.3:c.1428+1G>A , LRG_589t1:c.1428+1G>A	NP_000109.1:n.1428+1G>A
NM_001114753.2:c.1428+1G>A , LRG_589t2:c.1428+1G>A	NP_001108225.1:n.1428+1G>A
NM_001278138.1:c.882+1G>A	NP_001265067.1:n.882+1G>A
NR_136302.1:n.1568+4C>T
NM_001114753.3:c.1428+1G>A MANE Select	NP_001108225.1:n.1428+1G>A
NM_001278138.2:c.882+1G>A	NP_001265067.1:n.882+1G>A