Canonical Allele Identifier: CA2740447669

Gene: NECTIN3

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.111122199_111122200insA , CM000665.2:g.111122199_111122200insA	GRCh38
NC_000003.11:g.110841046_110841047insA , CM000665.1:g.110841046_110841047insA	GRCh37
NC_000003.10:g.112323736_112323737insA	NCBI36
NG_029835.1:g.55441_55442insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000485303.6:c.878_879insA MANE Select	ENSP00000418070.1:p.Asp294Ter
ENST00000319792.7:c.878_879insA	ENSP00000321514.3:p.Asp294Ter
ENST00000485303.5:c.878_879insA	ENSP00000418070.1:p.Asp294Ter
ENST00000486596.5:c.579_580insA
ENST00000493615.5:c.809_810insA	ENSP00000420579.1:p.Asp271Ter
NM_001243286.1:c.878_879insA	NP_001230215.1:p.Asp294Ter
NM_001243288.1:c.809_810insA	NP_001230217.1:p.Asp271Ter
NM_015480.2:c.878_879insA	NP_056295.1:p.Asp294Ter
XM_005247322.3:c.878_879insA	XP_005247379.2:p.Asp294Ter
XM_011512662.1:c.971_972insA	XP_011510964.1:p.Asp325Ter
XM_011512663.1:c.971_972insA	XP_011510965.1:p.Asp325Ter
XM_011512664.1:c.809_810insA	XP_011510966.1:p.Asp271Ter
XM_011512665.1:c.971_972insA	XP_011510967.1:p.Asp325Ter
XM_011512666.1:c.971_972insA	XP_011510968.1:p.Asp325Ter
XM_011512667.1:c.242_243insA	XP_011510969.1:p.Asp82Ter
XR_924122.1:n.1201_1202insA
XM_017006123.1:c.971_972insA	XP_016861612.1:p.Asp325Ter
XM_017006124.1:c.833_834insA	XP_016861613.1:p.Asp279Ter
XM_017006125.1:c.809_810insA	XP_016861614.1:p.Asp271Ter
XM_017006126.1:c.878_879insA	XP_016861615.1:p.Asp294Ter
XM_017006127.2:c.242_243insA	XP_016861616.1:p.Asp82Ter
XR_002959508.1:n.1159_1160insA
XR_924122.2:n.1201_1202insA
NM_015480.3:c.878_879insA MANE Select	NP_056295.1:p.Asp294Ter
NM_001243286.2:c.878_879insA	NP_001230215.1:p.Asp294Ter
NM_001243288.2:c.809_810insA	NP_001230217.1:p.Asp271Ter