Canonical Allele Identifier: CA1393291273

Gene: NECTIN3

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.111122214C= , CM000665.2:g.111122214C=	GRCh38
NC_000003.11:g.110841061C= , CM000665.1:g.110841061C=	GRCh37
NC_000003.10:g.112323751C=	NCBI36
NG_029835.1:g.55456C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000485303.6:c.893C= MANE Select	ENSP00000418070.1:p.Pro298=
ENST00000319792.7:c.893C=	ENSP00000321514.3:p.Pro298=
ENST00000485303.5:c.893C=	ENSP00000418070.1:p.Pro298=
ENST00000486596.5:c.594C=
ENST00000493615.5:c.824C=	ENSP00000420579.1:p.Pro275=
NM_001243286.1:c.893C=	NP_001230215.1:p.Pro298=
NM_001243288.1:c.824C=	NP_001230217.1:p.Pro275=
NM_015480.2:c.893C=	NP_056295.1:p.Pro298=
XM_005247322.3:c.893C=	XP_005247379.2:p.Pro298=
XM_011512662.1:c.986C=	XP_011510964.1:p.Pro329=
XM_011512663.1:c.986C=	XP_011510965.1:p.Pro329=
XM_011512664.1:c.824C=	XP_011510966.1:p.Pro275=
XM_011512665.1:c.986C=	XP_011510967.1:p.Pro329=
XM_011512666.1:c.986C=	XP_011510968.1:p.Pro329=
XM_011512667.1:c.257C=	XP_011510969.1:p.Pro86=
XR_924122.1:n.1216C=
XM_017006123.1:c.986C=	XP_016861612.1:p.Pro329=
XM_017006124.1:c.848C=	XP_016861613.1:p.Pro283=
XM_017006125.1:c.824C=	XP_016861614.1:p.Pro275=
XM_017006126.1:c.893C=	XP_016861615.1:p.Pro298=
XM_017006127.2:c.257C=	XP_016861616.1:p.Pro86=
XR_002959508.1:n.1174C=
XR_924122.2:n.1216C=
NM_015480.3:c.893C= MANE Select	NP_056295.1:p.Pro298=
NM_001243286.2:c.893C=	NP_001230215.1:p.Pro298=
NM_001243288.2:c.824C=	NP_001230217.1:p.Pro275=