Canonical Allele Identifier: CA1879981983
Gene: ENG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127816037G= , CM000671.2:g.127816037G= GRCh38
NC_000009.11:g.130578316G= , CM000671.1:g.130578316G= GRCh37
NC_000009.10:g.129618137G= NCBI36
NG_009551.1:g.43732C= , LRG_589:g.43732C=
NG_023245.1:g.18163G=

Transcript Alleles

HGVS Amino-acid change
ENST00000480266.6:c.1212C= ENSP00000479015.1:p.Gly404=
ENST00000373203.9:c.1758C= MANE Select ENSP00000362299.4:p.Gly586=
ENST00000344849.4:c.1758C= ENSP00000341917.3:p.Gly586=
ENST00000373203.8:c.1758C= ENSP00000362299.4:p.Gly586=
ENST00000480266.5:c.1212C= ENSP00000479015.1:p.Gly404=
NM_000118.3:c.1758C= , LRG_589t1:c.1758C= NP_000109.1:p.Gly586=
NM_001114753.2:c.1758C= , LRG_589t2:c.1758C= NP_001108225.1:p.Gly586=
NM_001278138.1:c.1212C= NP_001265067.1:p.Gly404=
NM_001114753.3:c.1758C= MANE Select NP_001108225.1:p.Gly586=
NM_001278138.2:c.1212C= NP_001265067.1:p.Gly404=