Canonical Allele Identifier: CA383281851
Gene: NECTIN1 HGNC NCBI

Linked Data

dbSNP Id: rs1485290152

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119677638C>G , CM000673.2:g.119677638C>G GRCh38
NC_000011.9:g.119548348C>G , CM000673.1:g.119548348C>G GRCh37
NC_000011.8:g.119053558C>G NCBI36
NG_013083.1:g.56088G>C
NG_013083.2:g.56088G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000531468.2:c.650G>C ENSP00000513010.1:p.Arg217Thr
ENST00000264025.8:c.650G>C MANE Select ENSP00000264025.3:p.Arg217Thr
ENST00000264025.7:c.650G>C ENSP00000264025.3:p.Arg217Thr
ENST00000340882.2:c.650G>C ENSP00000345289.2:p.Arg217Thr
ENST00000341398.6:c.650G>C ENSP00000344974.2:p.Arg217Thr
ENST00000524510.1:n.624G>C
NM_002855.4:c.650G>C NP_002846.3:p.Arg217Thr
NM_203285.1:c.650G>C NP_976030.1:p.Arg217Thr
NM_203286.1:c.650G>C NP_976031.1:p.Arg217Thr
NM_002855.5:c.650G>C MANE Select NP_002846.3:p.Arg217Thr
NM_203285.2:c.650G>C NP_976030.1:p.Arg217Thr
NM_203286.2:c.650G>C NP_976031.1:p.Arg217Thr