Canonical Allele Identifier: CA467474669

Gene: ENG

Linked Data

• MyVariant Identifiers: chr9:g.130587206A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127824927A>G , CM000671.2:g.127824927A>G	GRCh38
NC_000009.11:g.130587206A>G , CM000671.1:g.130587206A>G	GRCh37
NC_000009.10:g.129627027A>G	NCBI36
NG_009551.1:g.34842T>C , LRG_589:g.34842T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.318T>C	ENSP00000479015.1:p.Arg106=
ENST00000373203.9:c.864T>C MANE Select	ENSP00000362299.4:p.Arg288=
ENST00000344849.4:c.864T>C	ENSP00000341917.3:p.Arg288=
ENST00000373203.8:c.864T>C	ENSP00000362299.4:p.Arg288=
ENST00000480266.5:c.318T>C	ENSP00000479015.1:p.Arg106=
NM_000118.3:c.864T>C , LRG_589t1:c.864T>C	NP_000109.1:p.Arg288=
NM_001114753.2:c.864T>C , LRG_589t2:c.864T>C	NP_001108225.1:p.Arg288=
NM_001278138.1:c.318T>C	NP_001265067.1:p.Arg106=
NM_001114753.3:c.864T>C MANE Select	NP_001108225.1:p.Arg288=
NM_001278138.2:c.318T>C	NP_001265067.1:p.Arg106=