Canonical Allele Identifier: CA602586177

Gene: NECTIN1

Linked Data

• dbSNP Id: rs1263298270
• gnomAD v2: 11-119548201-A-AGGAGGAG
• gnomAD v3: 11-119677491-A-AGGAGGAG
• gnomAD v4: 11-119677491-A-AGGAGGAG
• MyVariant Identifiers: chr11:g.119548201_119548202insGGAGGAG (hg19) ; chr11:g.119677491_119677492insGGAGGAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119677502_119677508dup , CM000673.2:g.119677502_119677508dup	GRCh38
NC_000011.9:g.119548212_119548218dup , CM000673.1:g.119548212_119548218dup	GRCh37
NC_000011.8:g.119053422_119053428dup	NCBI36
NG_013083.1:g.56228_56234dup
NG_013083.2:g.56228_56234dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531468.2:c.733+57_733+63dup	ENSP00000513010.1:n.733+57_733+63dup
ENST00000264025.8:c.733+57_733+63dup MANE Select	ENSP00000264025.3:n.733+57_733+63dup
ENST00000264025.7:c.733+57_733+63dup	ENSP00000264025.3:n.733+57_733+63dup
ENST00000340882.2:c.733+57_733+63dup	ENSP00000345289.2:n.733+57_733+63dup
ENST00000341398.6:c.733+57_733+63dup	ENSP00000344974.2:n.733+57_733+63dup
ENST00000524510.1:n.707+57_707+63dup
ENST00000532197.1:n.47+57_47+63dup
NM_002855.4:c.733+57_733+63dup	NP_002846.3:n.733+57_733+63dup
NM_203285.1:c.733+57_733+63dup	NP_976030.1:n.733+57_733+63dup
NM_203286.1:c.733+57_733+63dup	NP_976031.1:n.733+57_733+63dup
NM_002855.5:c.733+57_733+63dup MANE Select	NP_002846.3:n.733+57_733+63dup
NM_203285.2:c.733+57_733+63dup	NP_976030.1:n.733+57_733+63dup
NM_203286.2:c.733+57_733+63dup	NP_976031.1:n.733+57_733+63dup