Canonical Allele Identifier: CA1393291222

Gene: NECTIN3

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.111122150G= , CM000665.2:g.111122150G=	GRCh38
NC_000003.11:g.110840997G= , CM000665.1:g.110840997G=	GRCh37
NC_000003.10:g.112323687G=	NCBI36
NG_029835.1:g.55392G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000485303.6:c.829G= MANE Select	ENSP00000418070.1:p.Asp277=
ENST00000319792.7:c.829G=	ENSP00000321514.3:p.Asp277=
ENST00000485303.5:c.829G=	ENSP00000418070.1:p.Asp277=
ENST00000486596.5:c.530G=
ENST00000493615.5:c.760G=	ENSP00000420579.1:p.Asp254=
NM_001243286.1:c.829G=	NP_001230215.1:p.Asp277=
NM_001243288.1:c.760G=	NP_001230217.1:p.Asp254=
NM_015480.2:c.829G=	NP_056295.1:p.Asp277=
XM_005247322.3:c.829G=	XP_005247379.2:p.Asp277=
XM_011512662.1:c.922G=	XP_011510964.1:p.Asp308=
XM_011512663.1:c.922G=	XP_011510965.1:p.Asp308=
XM_011512664.1:c.760G=	XP_011510966.1:p.Asp254=
XM_011512665.1:c.922G=	XP_011510967.1:p.Asp308=
XM_011512666.1:c.922G=	XP_011510968.1:p.Asp308=
XM_011512667.1:c.193G=	XP_011510969.1:p.Asp65=
XR_924122.1:n.1152G=
XM_017006123.1:c.922G=	XP_016861612.1:p.Asp308=
XM_017006124.1:c.784G=	XP_016861613.1:p.Asp262=
XM_017006125.1:c.760G=	XP_016861614.1:p.Asp254=
XM_017006126.1:c.829G=	XP_016861615.1:p.Asp277=
XM_017006127.2:c.193G=	XP_016861616.1:p.Asp65=
XR_002959508.1:n.1110G=
XR_924122.2:n.1152G=
NM_015480.3:c.829G= MANE Select	NP_056295.1:p.Asp277=
NM_001243286.2:c.829G=	NP_001230215.1:p.Asp277=
NM_001243288.2:c.760G=	NP_001230217.1:p.Asp254=