Canonical Allele Identifier: CA1879982670
Gene: ENG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127816478T= , CM000671.2:g.127816478T= GRCh38
NC_000009.11:g.130578757T= , CM000671.1:g.130578757T= GRCh37
NC_000009.10:g.129618578T= NCBI36
NG_009551.1:g.43291A= , LRG_589:g.43291A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000480266.6:c.1196-425A= ENSP00000479015.1:n.1196-425A=
ENST00000373203.9:c.1742-425A= MANE Select ENSP00000362299.4:n.1742-425A=
ENST00000344849.4:c.1742-425A= ENSP00000341917.3:n.1742-425A=
ENST00000373203.8:c.1742-425A= ENSP00000362299.4:n.1742-425A=
ENST00000480266.5:c.1196-425A= ENSP00000479015.1:n.1196-425A=
NM_000118.3:c.1742-425A= , LRG_589t1:c.1742-425A= NP_000109.1:n.1742-425A=
NM_001114753.2:c.1742-425A= , LRG_589t2:c.1742-425A= NP_001108225.1:n.1742-425A=
NM_001278138.1:c.1196-425A= NP_001265067.1:n.1196-425A=
XM_011519273.1:c.-101T= XP_011517575.1:n.-101T=
NR_136302.1:n.413T=
NM_001114753.3:c.1742-425A= MANE Select NP_001108225.1:n.1742-425A=
NM_001278138.2:c.1196-425A= NP_001265067.1:n.1196-425A=
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