Canonical Allele Identifier: CA2533835
Gene: NECTIN3 HGNC NCBI

Linked Data

dbSNP Id: rs779483747

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.111122252_111122253insATGATAAAATATTAAGATAATAGACAAAGCC , CM000665.2:g.111122252_111122253insATGATAAAATATTAAGATAATAGACAAAGCC GRCh38
NC_000003.11:g.110841099_110841100insATGATAAAATATTAAGATAATAGACAAAGCC , CM000665.1:g.110841099_110841100insATGATAAAATATTAAGATAATAGACAAAGCC GRCh37
NC_000003.10:g.112323789_112323790insATGATAAAATATTAAGATAATAGACAAAGCC NCBI36
NG_029835.1:g.55494_55495insATGATAAAATATTAAGATAATAGACAAAGCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000485303.6:c.917+14_917+15insATGATAAAATATTAAGATAATAGACAAAGCC MANE Select ENSP00000418070.1:n.917+14_917+15insATGATAAAATATTAAGATAATAGAC...
ENST00000319792.7:c.917+14_917+15insATGATAAAATATTAAGATAATAGACAAAGCC ENSP00000321514.3:n.917+14_917+15insATGATAAAATATTAAGATAATAGAC...
ENST00000485303.5:c.917+14_917+15insATGATAAAATATTAAGATAATAGACAAAGCC ENSP00000418070.1:n.917+14_917+15insATGATAAAATATTAAGATAATAGAC...
ENST00000486596.5:c.618+14_618+15insATGATAAAATATTAAGATAATAGACAAAGCC
ENST00000493615.5:c.848+14_848+15insATGATAAAATATTAAGATAATAGACAAAGCC ENSP00000420579.1:n.848+14_848+15insATGATAAAATATTAAGATAATAGAC...
NM_001243286.1:c.917+14_917+15insATGATAAAATATTAAGATAATAGACAAAGCC NP_001230215.1:n.917+14_917+15insATGATAAAATATTAAGATAATAGACAAA...
NM_001243288.1:c.848+14_848+15insATGATAAAATATTAAGATAATAGACAAAGCC NP_001230217.1:n.848+14_848+15insATGATAAAATATTAAGATAATAGACAAA...
NM_015480.2:c.917+14_917+15insATGATAAAATATTAAGATAATAGACAAAGCC NP_056295.1:n.917+14_917+15insATGATAAAATATTAAGATAATAGACAAAGCC...
XM_005247322.3:c.917+14_917+15insATGATAAAATATTAAGATAATAGACAAAGCC XP_005247379.2:n.917+14_917+15insATGATAAAATATTAAGATAATAGACAAA...
XM_011512662.1:c.1010+14_1010+15insATGATAAAATATTAAGATAATAGACAAAGCC XP_011510964.1:n.1010+14_1010+15insATGATAAAATATTAAGATAATAGACA...
XM_011512663.1:c.1010+14_1010+15insATGATAAAATATTAAGATAATAGACAAAGCC XP_011510965.1:n.1010+14_1010+15insATGATAAAATATTAAGATAATAGACA...
XM_011512664.1:c.848+14_848+15insATGATAAAATATTAAGATAATAGACAAAGCC XP_011510966.1:n.848+14_848+15insATGATAAAATATTAAGATAATAGACAAA...
XM_011512665.1:c.1010+14_1010+15insATGATAAAATATTAAGATAATAGACAAAGCC XP_011510967.1:n.1010+14_1010+15insATGATAAAATATTAAGATAATAGACA...
XM_011512666.1:c.1010+14_1010+15insATGATAAAATATTAAGATAATAGACAAAGCC XP_011510968.1:n.1010+14_1010+15insATGATAAAATATTAAGATAATAGACA...
XM_011512667.1:c.281+14_281+15insATGATAAAATATTAAGATAATAGACAAAGCC XP_011510969.1:n.281+14_281+15insATGATAAAATATTAAGATAATAGACAAA...
XR_924122.1:n.1240+14_1240+15insATGATAAAATATTAAGATAATAGACAAAGCC
XM_017006123.1:c.1010+14_1010+15insATGATAAAATATTAAGATAATAGACAAAGCC XP_016861612.1:n.1010+14_1010+15insATGATAAAATATTAAGATAATAGACA...
XM_017006124.1:c.872+14_872+15insATGATAAAATATTAAGATAATAGACAAAGCC XP_016861613.1:n.872+14_872+15insATGATAAAATATTAAGATAATAGACAAA...
XM_017006125.1:c.848+14_848+15insATGATAAAATATTAAGATAATAGACAAAGCC XP_016861614.1:n.848+14_848+15insATGATAAAATATTAAGATAATAGACAAA...
XM_017006126.1:c.917+14_917+15insATGATAAAATATTAAGATAATAGACAAAGCC XP_016861615.1:n.917+14_917+15insATGATAAAATATTAAGATAATAGACAAA...
XM_017006127.2:c.281+14_281+15insATGATAAAATATTAAGATAATAGACAAAGCC XP_016861616.1:n.281+14_281+15insATGATAAAATATTAAGATAATAGACAAA...
XR_002959508.1:n.1198+14_1198+15insATGATAAAATATTAAGATAATAGACAAAGCC
XR_924122.2:n.1240+14_1240+15insATGATAAAATATTAAGATAATAGACAAAGCC
NM_015480.3:c.917+14_917+15insATGATAAAATATTAAGATAATAGACAAAGCC MANE Select NP_056295.1:n.917+14_917+15insATGATAAAATATTAAGATAATAGACAAAGCC...
NM_001243286.2:c.917+14_917+15insATGATAAAATATTAAGATAATAGACAAAGCC NP_001230215.1:n.917+14_917+15insATGATAAAATATTAAGATAATAGACAAA...
NM_001243288.2:c.848+14_848+15insATGATAAAATATTAAGATAATAGACAAAGCC NP_001230217.1:n.848+14_848+15insATGATAAAATATTAAGATAATAGACAAA...