Canonical Allele Identifier: CA1879973182
Gene: ENG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127824731T= , CM000671.2:g.127824731T= GRCh38
NC_000009.11:g.130587010T= , CM000671.1:g.130587010T= GRCh37
NC_000009.10:g.129626831T= NCBI36
NG_009551.1:g.35038A= , LRG_589:g.35038A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000480266.6:c.445+69A= ENSP00000479015.1:n.445+69A=
ENST00000373203.9:c.991+69A= MANE Select ENSP00000362299.4:n.991+69A=
ENST00000344849.4:c.991+69A= ENSP00000341917.3:n.991+69A=
ENST00000373203.8:c.991+69A= ENSP00000362299.4:n.991+69A=
ENST00000480266.5:c.445+69A= ENSP00000479015.1:n.445+69A=
NM_000118.3:c.991+69A= , LRG_589t1:c.991+69A= NP_000109.1:n.991+69A=
NM_001114753.2:c.991+69A= , LRG_589t2:c.991+69A= NP_001108225.1:n.991+69A=
NM_001278138.1:c.445+69A= NP_001265067.1:n.445+69A=
NM_001114753.3:c.991+69A= MANE Select NP_001108225.1:n.991+69A=
NM_001278138.2:c.445+69A= NP_001265067.1:n.445+69A=