Canonical Allele Identifier: CA10575505
Gene: NECTIN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 8970
ClinVar RCV Id: RCV000009533
dbSNP Id: rs876657374

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119677734del , CM000673.2:g.119677734del GRCh38
NC_000011.9:g.119548444del , CM000673.1:g.119548444del GRCh37
NC_000011.8:g.119053654del NCBI36
NG_013083.1:g.55994del
NG_013083.2:g.55994del

Transcript Alleles

HGVS Amino-acid change
ENST00000531468.2:c.556del ENSP00000513010.1:p.Glu186LysfsTer4
ENST00000264025.8:c.556del MANE Select ENSP00000264025.3:p.Glu186LysfsTer4
ENST00000264025.7:c.556del ENSP00000264025.3:p.Glu186LysfsTer4
ENST00000340882.2:c.556del ENSP00000345289.2:p.Glu186LysfsTer4
ENST00000341398.6:c.556del ENSP00000344974.2:p.Glu186LysfsTer4
ENST00000524510.1:n.530del
NM_002855.4:c.556del NP_002846.3:p.Glu186LysfsTer4
NM_203285.1:c.556del NP_976030.1:p.Glu186LysfsTer4
NM_203286.1:c.556del NP_976031.1:p.Glu186LysfsTer4
NM_002855.5:c.556del MANE Select NP_002846.3:p.Glu186LysfsTer4
NM_203285.2:c.556del NP_976030.1:p.Glu186LysfsTer4
NM_203286.2:c.556del NP_976031.1:p.Glu186LysfsTer4