Canonical Allele Identifier: CA2004078803
Gene: NECTIN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119677642T= , CM000673.2:g.119677642T= GRCh38
NC_000011.9:g.119548352T= , CM000673.1:g.119548352T= GRCh37
NC_000011.8:g.119053562T= NCBI36
NG_013083.1:g.56084A=
NG_013083.2:g.56084A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000531468.2:c.646A= ENSP00000513010.1:p.Ser216=
ENST00000264025.8:c.646A= MANE Select ENSP00000264025.3:p.Ser216=
ENST00000264025.7:c.646A= ENSP00000264025.3:p.Ser216=
ENST00000340882.2:c.646A= ENSP00000345289.2:p.Ser216=
ENST00000341398.6:c.646A= ENSP00000344974.2:p.Ser216=
ENST00000524510.1:n.620A=
NM_002855.4:c.646A= NP_002846.3:p.Ser216=
NM_203285.1:c.646A= NP_976030.1:p.Ser216=
NM_203286.1:c.646A= NP_976031.1:p.Ser216=
NM_002855.5:c.646A= MANE Select NP_002846.3:p.Ser216=
NM_203285.2:c.646A= NP_976030.1:p.Ser216=
NM_203286.2:c.646A= NP_976031.1:p.Ser216=