Canonical Allele Identifier: CA1879981974
Gene: ENG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127816036G= , CM000671.2:g.127816036G= GRCh38
NC_000009.11:g.130578315G= , CM000671.1:g.130578315G= GRCh37
NC_000009.10:g.129618136G= NCBI36
NG_009551.1:g.43733C= , LRG_589:g.43733C=
NG_023245.1:g.18162G=

Transcript Alleles

HGVS Amino-acid change
ENST00000480266.6:c.1213C= ENSP00000479015.1:p.Leu405=
ENST00000373203.9:c.1759C= MANE Select ENSP00000362299.4:p.Leu587=
ENST00000344849.4:c.1759C= ENSP00000341917.3:p.Leu587=
ENST00000373203.8:c.1759C= ENSP00000362299.4:p.Leu587=
ENST00000480266.5:c.1213C= ENSP00000479015.1:p.Leu405=
NM_000118.3:c.1759C= , LRG_589t1:c.1759C= NP_000109.1:p.Leu587=
NM_001114753.2:c.1759C= , LRG_589t2:c.1759C= NP_001108225.1:p.Leu587=
NM_001278138.1:c.1213C= NP_001265067.1:p.Leu405=
NM_001114753.3:c.1759C= MANE Select NP_001108225.1:p.Leu587=
NM_001278138.2:c.1213C= NP_001265067.1:p.Leu405=