Canonical Allele Identifier: CA374971424

Gene: ENG

Linked Data

• MyVariant Identifiers: chr9:g.130578216A>G (hg19) ; chr9:g.127815937A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127815937A>G , CM000671.2:g.127815937A>G	GRCh38
NC_000009.11:g.130578216A>G , CM000671.1:g.130578216A>G	GRCh37
NC_000009.10:g.129618037A>G	NCBI36
NG_009551.1:g.43832T>C , LRG_589:g.43832T>C
NG_023245.1:g.18063A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000480266.6:c.1306+6T>C	ENSP00000479015.1:n.1306+6T>C
ENST00000373203.9:c.1852+6T>C MANE Select	ENSP00000362299.4:n.1852+6T>C
ENST00000344849.4:c.1858T>C	ENSP00000341917.3:p.Tyr620His
ENST00000373203.8:c.1852+6T>C	ENSP00000362299.4:n.1852+6T>C
ENST00000480266.5:c.1306+6T>C	ENSP00000479015.1:n.1306+6T>C
NM_000118.3:c.1858T>C , LRG_589t1:c.1858T>C	NP_000109.1:p.Tyr620His
NM_001114753.2:c.1852+6T>C , LRG_589t2:c.1852+6T>C	NP_001108225.1:n.1852+6T>C
NM_001278138.1:c.1306+6T>C	NP_001265067.1:n.1306+6T>C
NM_001114753.3:c.1852+6T>C MANE Select	NP_001108225.1:n.1852+6T>C
NM_001278138.2:c.1306+6T>C	NP_001265067.1:n.1306+6T>C