Canonical Allele Identifier: CA860194280

Gene: ENG

Linked Data

• dbSNP Id: rs1346937091
• MyVariant Identifiers: chr9:g.130582558C>T (hg19) ; chr9:g.127820279C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127820279C>T , CM000671.2:g.127820279C>T	GRCh38
NC_000009.11:g.130582558C>T , CM000671.1:g.130582558C>T	GRCh37
NC_000009.10:g.129622379C>T	NCBI36
NG_009551.1:g.39490G>A , LRG_589:g.39490G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.589-242G>A	ENSP00000479015.1:n.589-242G>A
ENST00000373203.9:c.1135-242G>A MANE Select	ENSP00000362299.4:n.1135-242G>A
ENST00000344849.4:c.1135-242G>A	ENSP00000341917.3:n.1135-242G>A
ENST00000373203.8:c.1135-242G>A	ENSP00000362299.4:n.1135-242G>A
ENST00000480266.5:c.589-242G>A	ENSP00000479015.1:n.589-242G>A
ENST00000486329.1:n.103-242G>A
NM_000118.3:c.1135-242G>A , LRG_589t1:c.1135-242G>A	NP_000109.1:n.1135-242G>A
NM_001114753.2:c.1135-242G>A , LRG_589t2:c.1135-242G>A	NP_001108225.1:n.1135-242G>A
NM_001278138.1:c.589-242G>A	NP_001265067.1:n.589-242G>A
NR_136302.1:n.1569-916C>T
NM_001114753.3:c.1135-242G>A MANE Select	NP_001108225.1:n.1135-242G>A
NM_001278138.2:c.589-242G>A	NP_001265067.1:n.589-242G>A