Canonical Allele Identifier: CA2740447668

Gene: NECTIN3

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.111122196_111122197dup , CM000665.2:g.111122196_111122197dup	GRCh38
NC_000003.11:g.110841043_110841044dup , CM000665.1:g.110841043_110841044dup	GRCh37
NC_000003.10:g.112323733_112323734dup	NCBI36
NG_029835.1:g.55438_55439dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000485303.6:c.875_876dup MANE Select	ENSP00000418070.1:p.Ala293MetfsTer?
ENST00000319792.7:c.875_876dup	ENSP00000321514.3:p.Ala293MetfsTer?
ENST00000485303.5:c.875_876dup	ENSP00000418070.1:p.Ala293MetfsTer?
ENST00000486596.5:c.576_577dup
ENST00000493615.5:c.806_807dup	ENSP00000420579.1:p.Ala270MetfsTer?
NM_001243286.1:c.875_876dup	NP_001230215.1:p.Ala293MetfsTer?
NM_001243288.1:c.806_807dup	NP_001230217.1:p.Ala270MetfsTer?
NM_015480.2:c.875_876dup	NP_056295.1:p.Ala293MetfsTer?
XM_005247322.3:c.875_876dup	XP_005247379.2:p.Ala293MetfsTer?
XM_011512662.1:c.968_969dup	XP_011510964.1:p.Ala324MetfsTer?
XM_011512663.1:c.968_969dup	XP_011510965.1:p.Ala324MetfsTer?
XM_011512664.1:c.806_807dup	XP_011510966.1:p.Ala270MetfsTer?
XM_011512665.1:c.968_969dup	XP_011510967.1:p.Ala324MetfsTer?
XM_011512666.1:c.968_969dup	XP_011510968.1:p.Ala324MetfsTer?
XM_011512667.1:c.239_240dup	XP_011510969.1:p.Ala81MetfsTer?
XR_924122.1:n.1198_1199dup
XM_017006123.1:c.968_969dup	XP_016861612.1:p.Ala324MetfsTer?
XM_017006124.1:c.830_831dup	XP_016861613.1:p.Ala278MetfsTer?
XM_017006125.1:c.806_807dup	XP_016861614.1:p.Ala270MetfsTer?
XM_017006126.1:c.875_876dup	XP_016861615.1:p.Ala293MetfsTer?
XM_017006127.2:c.239_240dup	XP_016861616.1:p.Ala81MetfsTer?
XR_002959508.1:n.1156_1157dup
XR_924122.2:n.1198_1199dup
NM_015480.3:c.875_876dup MANE Select	NP_056295.1:p.Ala293MetfsTer?
NM_001243286.2:c.875_876dup	NP_001230215.1:p.Ala293MetfsTer?
NM_001243288.2:c.806_807dup	NP_001230217.1:p.Ala270MetfsTer?