Canonical Allele Identifier: CA2004078474
Gene: NECTIN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119677459A= , CM000673.2:g.119677459A= GRCh38
NC_000011.9:g.119548169A= , CM000673.1:g.119548169A= GRCh37
NC_000011.8:g.119053379A= NCBI36
NG_013083.1:g.56267T=
NG_013083.2:g.56267T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000531468.2:c.733+96T= ENSP00000513010.1:n.733+96T=
ENST00000264025.8:c.733+96T= MANE Select ENSP00000264025.3:n.733+96T=
ENST00000264025.7:c.733+96T= ENSP00000264025.3:n.733+96T=
ENST00000340882.2:c.733+96T= ENSP00000345289.2:n.733+96T=
ENST00000341398.6:c.733+96T= ENSP00000344974.2:n.733+96T=
ENST00000524510.1:n.707+96T=
ENST00000532197.1:n.47+96T=
NM_002855.4:c.733+96T= NP_002846.3:n.733+96T=
NM_203285.1:c.733+96T= NP_976030.1:n.733+96T=
NM_203286.1:c.733+96T= NP_976031.1:n.733+96T=
NM_002855.5:c.733+96T= MANE Select NP_002846.3:n.733+96T=
NM_203285.2:c.733+96T= NP_976030.1:n.733+96T=
NM_203286.2:c.733+96T= NP_976031.1:n.733+96T=