Canonical Allele Identifier: CA942815448

Gene: NECTIN1

Linked Data

• dbSNP Id: rs1864974463
• gnomAD v3: 11-119677485-AAGGAGAGGAGGAGGG-A
• gnomAD v4: 11-119677485-AAGGAGAGGAGGAGGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119677491_119677505del , CM000673.2:g.119677491_119677505del	GRCh38
NC_000011.9:g.119548201_119548215del , CM000673.1:g.119548201_119548215del	GRCh37
NC_000011.8:g.119053411_119053425del	NCBI36
NG_013083.1:g.56226_56240del
NG_013083.2:g.56226_56240del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531468.2:c.733+55_733+69del	ENSP00000513010.1:n.733+55_733+69del
ENST00000264025.8:c.733+55_733+69del MANE Select	ENSP00000264025.3:n.733+55_733+69del
ENST00000264025.7:c.733+55_733+69del	ENSP00000264025.3:n.733+55_733+69del
ENST00000340882.2:c.733+55_733+69del	ENSP00000345289.2:n.733+55_733+69del
ENST00000341398.6:c.733+55_733+69del	ENSP00000344974.2:n.733+55_733+69del
ENST00000524510.1:n.707+55_707+69del
ENST00000532197.1:n.47+55_47+69del
NM_002855.4:c.733+55_733+69del	NP_002846.3:n.733+55_733+69del
NM_203285.1:c.733+55_733+69del	NP_976030.1:n.733+55_733+69del
NM_203286.1:c.733+55_733+69del	NP_976031.1:n.733+55_733+69del
NM_002855.5:c.733+55_733+69del MANE Select	NP_002846.3:n.733+55_733+69del
NM_203285.2:c.733+55_733+69del	NP_976030.1:n.733+55_733+69del
NM_203286.2:c.733+55_733+69del	NP_976031.1:n.733+55_733+69del