Canonical Allele Identifier: CA383282202
Gene: NECTIN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119677806T>C , CM000673.2:g.119677806T>C GRCh38
NC_000011.9:g.119548516T>C , CM000673.1:g.119548516T>C GRCh37
NC_000011.8:g.119053726T>C NCBI36
NG_013083.1:g.55920A>G
NG_013083.2:g.55920A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000531468.2:c.482A>G ENSP00000513010.1:p.Lys161Arg
ENST00000264025.8:c.482A>G MANE Select ENSP00000264025.3:p.Lys161Arg
ENST00000264025.7:c.482A>G ENSP00000264025.3:p.Lys161Arg
ENST00000340882.2:c.482A>G ENSP00000345289.2:p.Lys161Arg
ENST00000341398.6:c.482A>G ENSP00000344974.2:p.Lys161Arg
ENST00000524510.1:n.456A>G
NM_002855.4:c.482A>G NP_002846.3:p.Lys161Arg
NM_203285.1:c.482A>G NP_976030.1:p.Lys161Arg
NM_203286.1:c.482A>G NP_976031.1:p.Lys161Arg
NM_002855.5:c.482A>G MANE Select NP_002846.3:p.Lys161Arg
NM_203285.2:c.482A>G NP_976030.1:p.Lys161Arg
NM_203286.2:c.482A>G NP_976031.1:p.Lys161Arg