Canonical Allele Identifier: CA942815636
Gene: NECTIN1 HGNC NCBI

Linked Data

dbSNP Id: rs1864989032

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119677946dup , CM000673.2:g.119677946dup GRCh38
NC_000011.9:g.119548656dup , CM000673.1:g.119548656dup GRCh37
NC_000011.8:g.119053866dup NCBI36
NG_013083.1:g.55781dup
NG_013083.2:g.55781dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000531468.2:c.431-88dup ENSP00000513010.1:n.431-88dup
ENST00000264025.8:c.431-88dup MANE Select ENSP00000264025.3:n.431-88dup
ENST00000264025.7:c.431-88dup ENSP00000264025.3:n.431-88dup
ENST00000340882.2:c.431-88dup ENSP00000345289.2:n.431-88dup
ENST00000341398.6:c.431-88dup ENSP00000344974.2:n.431-88dup
ENST00000524510.1:n.405-88dup
NM_002855.4:c.431-88dup NP_002846.3:n.431-88dup
NM_203285.1:c.431-88dup NP_976030.1:n.431-88dup
NM_203286.1:c.431-88dup NP_976031.1:n.431-88dup
NM_002855.5:c.431-88dup MANE Select NP_002846.3:n.431-88dup
NM_203285.2:c.431-88dup NP_976030.1:n.431-88dup
NM_203286.2:c.431-88dup NP_976031.1:n.431-88dup