Canonical Allele Identifier: CA2004078527

Gene: NECTIN1

Linked Data

• dbSNP Id: rs1864975254
• gnomAD v4: 11-119677509-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119677509C>G , CM000673.2:g.119677509C>G	GRCh38
NC_000011.9:g.119548219C>G , CM000673.1:g.119548219C>G	GRCh37
NC_000011.8:g.119053429C>G	NCBI36
NG_013083.1:g.56217G>C
NG_013083.2:g.56217G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531468.2:c.733+46G>C	ENSP00000513010.1:n.733+46G>C
ENST00000264025.8:c.733+46G>C MANE Select	ENSP00000264025.3:n.733+46G>C
ENST00000264025.7:c.733+46G>C	ENSP00000264025.3:n.733+46G>C
ENST00000340882.2:c.733+46G>C	ENSP00000345289.2:n.733+46G>C
ENST00000341398.6:c.733+46G>C	ENSP00000344974.2:n.733+46G>C
ENST00000524510.1:n.707+46G>C
ENST00000532197.1:n.47+46G>C
NM_002855.4:c.733+46G>C	NP_002846.3:n.733+46G>C
NM_203285.1:c.733+46G>C	NP_976030.1:n.733+46G>C
NM_203286.1:c.733+46G>C	NP_976031.1:n.733+46G>C
NM_002855.5:c.733+46G>C MANE Select	NP_002846.3:n.733+46G>C
NM_203285.2:c.733+46G>C	NP_976030.1:n.733+46G>C
NM_203286.2:c.733+46G>C	NP_976031.1:n.733+46G>C