Canonical Allele Identifier: CA374970703

Gene: ENG

Linked Data

• MyVariant Identifiers: chr9:g.130578066C>A (hg19) ; chr9:g.127815787C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127815787C>A , CM000671.2:g.127815787C>A	GRCh38
NC_000009.11:g.130578066C>A , CM000671.1:g.130578066C>A	GRCh37
NC_000009.10:g.129617887C>A	NCBI36
NG_009551.1:g.43982G>T , LRG_589:g.43982G>T
NG_023245.1:g.17913C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.1326G>T	ENSP00000479015.1:p.Glu442Asp
ENST00000373203.9:c.1872G>T MANE Select	ENSP00000362299.4:p.Glu624Asp
ENST00000344849.4:c.*130G>T	ENSP00000341917.3:n.*130G>T
ENST00000373203.8:c.1872G>T	ENSP00000362299.4:p.Glu624Asp
ENST00000480266.5:c.1326G>T	ENSP00000479015.1:p.Glu442Asp
NM_000118.3:c.*130G>T , LRG_589t1:c.*130G>T	NP_000109.1:n.*130G>T
NM_001114753.2:c.1872G>T , LRG_589t2:c.1872G>T	NP_001108225.1:p.Glu624Asp
NM_001278138.1:c.1326G>T	NP_001265067.1:p.Glu442Asp
NM_001114753.3:c.1872G>T MANE Select	NP_001108225.1:p.Glu624Asp
NM_001278138.2:c.1326G>T	NP_001265067.1:p.Glu442Asp