Canonical Allele Identifier: CA2004078815
Gene: NECTIN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119677643G= , CM000673.2:g.119677643G= GRCh38
NC_000011.9:g.119548353G= , CM000673.1:g.119548353G= GRCh37
NC_000011.8:g.119053563G= NCBI36
NG_013083.1:g.56083C=
NG_013083.2:g.56083C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000531468.2:c.645C= ENSP00000513010.1:p.Pro215=
ENST00000264025.8:c.645C= MANE Select ENSP00000264025.3:p.Pro215=
ENST00000264025.7:c.645C= ENSP00000264025.3:p.Pro215=
ENST00000340882.2:c.645C= ENSP00000345289.2:p.Pro215=
ENST00000341398.6:c.645C= ENSP00000344974.2:p.Pro215=
ENST00000524510.1:n.619C=
NM_002855.4:c.645C= NP_002846.3:p.Pro215=
NM_203285.1:c.645C= NP_976030.1:p.Pro215=
NM_203286.1:c.645C= NP_976031.1:p.Pro215=
NM_002855.5:c.645C= MANE Select NP_002846.3:p.Pro215=
NM_203285.2:c.645C= NP_976030.1:p.Pro215=
NM_203286.2:c.645C= NP_976031.1:p.Pro215=