Canonical Allele Identifier: CA2575044782
Gene: NECTIN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119677857del , CM000673.2:g.119677857del GRCh38
NC_000011.9:g.119548567del , CM000673.1:g.119548567del GRCh37
NC_000011.8:g.119053777del NCBI36
NG_013083.1:g.55870del
NG_013083.2:g.55870del

Transcript Alleles

HGVS Amino-acid Change
ENST00000531468.2:c.432del ENSP00000513010.1:p.Lys145AsnfsTer6
ENST00000264025.8:c.432del MANE Select ENSP00000264025.3:p.Lys145AsnfsTer6
ENST00000264025.7:c.432del ENSP00000264025.3:p.Lys145AsnfsTer6
ENST00000340882.2:c.432del ENSP00000345289.2:p.Lys145AsnfsTer6
ENST00000341398.6:c.432del ENSP00000344974.2:p.Lys145AsnfsTer6
ENST00000524510.1:n.406del
NM_002855.4:c.432del NP_002846.3:p.Lys145AsnfsTer6
NM_203285.1:c.432del NP_976030.1:p.Lys145AsnfsTer6
NM_203286.1:c.432del NP_976031.1:p.Lys145AsnfsTer6
NM_002855.5:c.432del MANE Select NP_002846.3:p.Lys145AsnfsTer6
NM_203285.2:c.432del NP_976030.1:p.Lys145AsnfsTer6
NM_203286.2:c.432del NP_976031.1:p.Lys145AsnfsTer6