Canonical Allele Identifier: CA1879998189
Gene: ENG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127853918C= , CM000671.2:g.127853918C= GRCh38
NC_000009.11:g.130616197C= , CM000671.1:g.130616197C= GRCh37
NC_000009.10:g.129656018C= NCBI36
NG_009551.1:g.5851G= , LRG_589:g.5851G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373203.9:c.67+371G= MANE Select ENSP00000362299.4:n.67+371G=
ENST00000344849.4:c.67+371G= ENSP00000341917.3:n.67+371G=
ENST00000373203.8:c.67+371G= ENSP00000362299.4:n.67+371G=
NM_000118.3:c.67+371G= , LRG_589t1:c.67+371G= NP_000109.1:n.67+371G=
NM_001114753.2:c.67+371G= , LRG_589t2:c.67+371G= NP_001108225.1:n.67+371G=
NM_001114753.3:c.67+371G= MANE Select NP_001108225.1:n.67+371G=
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