Canonical Allele Identifier: CA477265295
Gene: NECTIN1 HGNC NCBI

Linked Data

dbSNP Id: rs1864983799
MyVariant Identifiers: chr11:g.119548458G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119677748G>A , CM000673.2:g.119677748G>A GRCh38
NC_000011.9:g.119548458G>A , CM000673.1:g.119548458G>A GRCh37
NC_000011.8:g.119053668G>A NCBI36
NG_013083.1:g.55978C>T
NG_013083.2:g.55978C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000531468.2:c.540C>T ENSP00000513010.1:p.Pro180=
ENST00000264025.8:c.540C>T MANE Select ENSP00000264025.3:p.Pro180=
ENST00000264025.7:c.540C>T ENSP00000264025.3:p.Pro180=
ENST00000340882.2:c.540C>T ENSP00000345289.2:p.Pro180=
ENST00000341398.6:c.540C>T ENSP00000344974.2:p.Pro180=
ENST00000524510.1:n.514C>T
NM_002855.4:c.540C>T NP_002846.3:p.Pro180=
NM_203285.1:c.540C>T NP_976030.1:p.Pro180=
NM_203286.1:c.540C>T NP_976031.1:p.Pro180=
NM_002855.5:c.540C>T MANE Select NP_002846.3:p.Pro180=
NM_203285.2:c.540C>T NP_976030.1:p.Pro180=
NM_203286.2:c.540C>T NP_976031.1:p.Pro180=