Canonical Allele Identifier: CA2004079185
Gene: NECTIN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119677805C= , CM000673.2:g.119677805C= GRCh38
NC_000011.9:g.119548515C= , CM000673.1:g.119548515C= GRCh37
NC_000011.8:g.119053725C= NCBI36
NG_013083.1:g.55921G=
NG_013083.2:g.55921G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000531468.2:c.483G= ENSP00000513010.1:p.Lys161=
ENST00000264025.8:c.483G= MANE Select ENSP00000264025.3:p.Lys161=
ENST00000264025.7:c.483G= ENSP00000264025.3:p.Lys161=
ENST00000340882.2:c.483G= ENSP00000345289.2:p.Lys161=
ENST00000341398.6:c.483G= ENSP00000344974.2:p.Lys161=
ENST00000524510.1:n.457G=
NM_002855.4:c.483G= NP_002846.3:p.Lys161=
NM_203285.1:c.483G= NP_976030.1:p.Lys161=
NM_203286.1:c.483G= NP_976031.1:p.Lys161=
NM_002855.5:c.483G= MANE Select NP_002846.3:p.Lys161=
NM_203285.2:c.483G= NP_976030.1:p.Lys161=
NM_203286.2:c.483G= NP_976031.1:p.Lys161=