Canonical Allele Identifier: CA435181896

Gene: NECTIN3

Linked Data

• dbSNP Id: rs2107470769
• MyVariant Identifiers: chr3:g.110841005T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.111122158T>C , CM000665.2:g.111122158T>C	GRCh38
NC_000003.11:g.110841005T>C , CM000665.1:g.110841005T>C	GRCh37
NC_000003.10:g.112323695T>C	NCBI36
NG_029835.1:g.55400T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000485303.6:c.837T>C MANE Select	ENSP00000418070.1:p.Asn279=
ENST00000319792.7:c.837T>C	ENSP00000321514.3:p.Asn279=
ENST00000485303.5:c.837T>C	ENSP00000418070.1:p.Asn279=
ENST00000486596.5:c.538T>C
ENST00000493615.5:c.768T>C	ENSP00000420579.1:p.Asn256=
NM_001243286.1:c.837T>C	NP_001230215.1:p.Asn279=
NM_001243288.1:c.768T>C	NP_001230217.1:p.Asn256=
NM_015480.2:c.837T>C	NP_056295.1:p.Asn279=
XM_005247322.3:c.837T>C	XP_005247379.2:p.Asn279=
XM_011512662.1:c.930T>C	XP_011510964.1:p.Asn310=
XM_011512663.1:c.930T>C	XP_011510965.1:p.Asn310=
XM_011512664.1:c.768T>C	XP_011510966.1:p.Asn256=
XM_011512665.1:c.930T>C	XP_011510967.1:p.Asn310=
XM_011512666.1:c.930T>C	XP_011510968.1:p.Asn310=
XM_011512667.1:c.201T>C	XP_011510969.1:p.Asn67=
XR_924122.1:n.1160T>C
XM_017006123.1:c.930T>C	XP_016861612.1:p.Asn310=
XM_017006124.1:c.792T>C	XP_016861613.1:p.Asn264=
XM_017006125.1:c.768T>C	XP_016861614.1:p.Asn256=
XM_017006126.1:c.837T>C	XP_016861615.1:p.Asn279=
XM_017006127.2:c.201T>C	XP_016861616.1:p.Asn67=
XR_002959508.1:n.1118T>C
XR_924122.2:n.1160T>C
NM_015480.3:c.837T>C MANE Select	NP_056295.1:p.Asn279=
NM_001243286.2:c.837T>C	NP_001230215.1:p.Asn279=
NM_001243288.2:c.768T>C	NP_001230217.1:p.Asn256=