Canonical Allele Identifier: CA383281766
Gene: NECTIN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119677600A>T , CM000673.2:g.119677600A>T GRCh38
NC_000011.9:g.119548310A>T , CM000673.1:g.119548310A>T GRCh37
NC_000011.8:g.119053520A>T NCBI36
NG_013083.1:g.56126T>A
NG_013083.2:g.56126T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000531468.2:c.688T>A ENSP00000513010.1:p.Tyr230Asn
ENST00000264025.8:c.688T>A MANE Select ENSP00000264025.3:p.Tyr230Asn
ENST00000264025.7:c.688T>A ENSP00000264025.3:p.Tyr230Asn
ENST00000340882.2:c.688T>A ENSP00000345289.2:p.Tyr230Asn
ENST00000341398.6:c.688T>A ENSP00000344974.2:p.Tyr230Asn
ENST00000524510.1:n.662T>A
ENST00000532197.1:n.2T>A
NM_002855.4:c.688T>A NP_002846.3:p.Tyr230Asn
NM_203285.1:c.688T>A NP_976030.1:p.Tyr230Asn
NM_203286.1:c.688T>A NP_976031.1:p.Tyr230Asn
NM_002855.5:c.688T>A MANE Select NP_002846.3:p.Tyr230Asn
NM_203285.2:c.688T>A NP_976030.1:p.Tyr230Asn
NM_203286.2:c.688T>A NP_976031.1:p.Tyr230Asn