Canonical Allele Identifier: CA353984683

Gene: NECTIN3

Linked Data

• MyVariant Identifiers: chr3:g.110841031A>G (hg19) ; chr3:g.111122184A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.111122184A>G , CM000665.2:g.111122184A>G	GRCh38
NC_000003.11:g.110841031A>G , CM000665.1:g.110841031A>G	GRCh37
NC_000003.10:g.112323721A>G	NCBI36
NG_029835.1:g.55426A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000485303.6:c.863A>G MANE Select	ENSP00000418070.1:p.Asn288Ser
ENST00000319792.7:c.863A>G	ENSP00000321514.3:p.Asn288Ser
ENST00000485303.5:c.863A>G	ENSP00000418070.1:p.Asn288Ser
ENST00000486596.5:c.564A>G
ENST00000493615.5:c.794A>G	ENSP00000420579.1:p.Asn265Ser
NM_001243286.1:c.863A>G	NP_001230215.1:p.Asn288Ser
NM_001243288.1:c.794A>G	NP_001230217.1:p.Asn265Ser
NM_015480.2:c.863A>G	NP_056295.1:p.Asn288Ser
XM_005247322.3:c.863A>G	XP_005247379.2:p.Asn288Ser
XM_011512662.1:c.956A>G	XP_011510964.1:p.Asn319Ser
XM_011512663.1:c.956A>G	XP_011510965.1:p.Asn319Ser
XM_011512664.1:c.794A>G	XP_011510966.1:p.Asn265Ser
XM_011512665.1:c.956A>G	XP_011510967.1:p.Asn319Ser
XM_011512666.1:c.956A>G	XP_011510968.1:p.Asn319Ser
XM_011512667.1:c.227A>G	XP_011510969.1:p.Asn76Ser
XR_924122.1:n.1186A>G
XM_017006123.1:c.956A>G	XP_016861612.1:p.Asn319Ser
XM_017006124.1:c.818A>G	XP_016861613.1:p.Asn273Ser
XM_017006125.1:c.794A>G	XP_016861614.1:p.Asn265Ser
XM_017006126.1:c.863A>G	XP_016861615.1:p.Asn288Ser
XM_017006127.2:c.227A>G	XP_016861616.1:p.Asn76Ser
XR_002959508.1:n.1144A>G
XR_924122.2:n.1186A>G
NM_015480.3:c.863A>G MANE Select	NP_056295.1:p.Asn288Ser
NM_001243286.2:c.863A>G	NP_001230215.1:p.Asn288Ser
NM_001243288.2:c.794A>G	NP_001230217.1:p.Asn265Ser