Canonical Allele Identifier: CA374970713

Gene: ENG

Linked Data

• MyVariant Identifiers: chr9:g.130578067T>G (hg19) ; chr9:g.127815788T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127815788T>G , CM000671.2:g.127815788T>G	GRCh38
NC_000009.11:g.130578067T>G , CM000671.1:g.130578067T>G	GRCh37
NC_000009.10:g.129617888T>G	NCBI36
NG_009551.1:g.43981A>C , LRG_589:g.43981A>C
NG_023245.1:g.17914T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.1325A>C	ENSP00000479015.1:p.Glu442Ala
ENST00000373203.9:c.1871A>C MANE Select	ENSP00000362299.4:p.Glu624Ala
ENST00000344849.4:c.*129A>C	ENSP00000341917.3:n.*129A>C
ENST00000373203.8:c.1871A>C	ENSP00000362299.4:p.Glu624Ala
ENST00000480266.5:c.1325A>C	ENSP00000479015.1:p.Glu442Ala
NM_000118.3:c.*129A>C , LRG_589t1:c.*129A>C	NP_000109.1:n.*129A>C
NM_001114753.2:c.1871A>C , LRG_589t2:c.1871A>C	NP_001108225.1:p.Glu624Ala
NM_001278138.1:c.1325A>C	NP_001265067.1:p.Glu442Ala
NM_001114753.3:c.1871A>C MANE Select	NP_001108225.1:p.Glu624Ala
NM_001278138.2:c.1325A>C	NP_001265067.1:p.Glu442Ala