Canonical Allele Identifier: CA1879998631
Gene: ENG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127854279G= , CM000671.2:g.127854279G= GRCh38
NC_000009.11:g.130616558G= , CM000671.1:g.130616558G= GRCh37
NC_000009.10:g.129656379G= NCBI36
NG_009551.1:g.5490C= , LRG_589:g.5490C=

Transcript Alleles

HGVS Amino-acid change
ENST00000373203.9:c.67+10C= MANE Select ENSP00000362299.4:n.67+10C=
ENST00000344849.4:c.67+10C= ENSP00000341917.3:n.67+10C=
ENST00000373203.8:c.67+10C= ENSP00000362299.4:n.67+10C=
NM_000118.3:c.67+10C= , LRG_589t1:c.67+10C= NP_000109.1:n.67+10C=
NM_001114753.2:c.67+10C= , LRG_589t2:c.67+10C= NP_001108225.1:n.67+10C=
NM_001114753.3:c.67+10C= MANE Select NP_001108225.1:n.67+10C=