Canonical Allele Identifier: CA353984800

Gene: NECTIN3

Linked Data

• gnomAD v4: 3-111122236-C-A
• MyVariant Identifiers: chr3:g.110841083C>A (hg19) ; chr3:g.111122236C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.111122236C>A , CM000665.2:g.111122236C>A	GRCh38
NC_000003.11:g.110841083C>A , CM000665.1:g.110841083C>A	GRCh37
NC_000003.10:g.112323773C>A	NCBI36
NG_029835.1:g.55478C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000485303.6:c.915C>A MANE Select	ENSP00000418070.1:p.Ser305Arg
ENST00000319792.7:c.915C>A	ENSP00000321514.3:p.Ser305Arg
ENST00000485303.5:c.915C>A	ENSP00000418070.1:p.Ser305Arg
ENST00000486596.5:c.616C>A
ENST00000493615.5:c.846C>A	ENSP00000420579.1:p.Ser282Arg
NM_001243286.1:c.915C>A	NP_001230215.1:p.Ser305Arg
NM_001243288.1:c.846C>A	NP_001230217.1:p.Ser282Arg
NM_015480.2:c.915C>A	NP_056295.1:p.Ser305Arg
XM_005247322.3:c.915C>A	XP_005247379.2:p.Ser305Arg
XM_011512662.1:c.1008C>A	XP_011510964.1:p.Ser336Arg
XM_011512663.1:c.1008C>A	XP_011510965.1:p.Ser336Arg
XM_011512664.1:c.846C>A	XP_011510966.1:p.Ser282Arg
XM_011512665.1:c.1008C>A	XP_011510967.1:p.Ser336Arg
XM_011512666.1:c.1008C>A	XP_011510968.1:p.Ser336Arg
XM_011512667.1:c.279C>A	XP_011510969.1:p.Ser93Arg
XR_924122.1:n.1238C>A
XM_017006123.1:c.1008C>A	XP_016861612.1:p.Ser336Arg
XM_017006124.1:c.870C>A	XP_016861613.1:p.Ser290Arg
XM_017006125.1:c.846C>A	XP_016861614.1:p.Ser282Arg
XM_017006126.1:c.915C>A	XP_016861615.1:p.Ser305Arg
XM_017006127.2:c.279C>A	XP_016861616.1:p.Ser93Arg
XR_002959508.1:n.1196C>A
XR_924122.2:n.1238C>A
NM_015480.3:c.915C>A MANE Select	NP_056295.1:p.Ser305Arg
NM_001243286.2:c.915C>A	NP_001230215.1:p.Ser305Arg
NM_001243288.2:c.846C>A	NP_001230217.1:p.Ser282Arg