Canonical Allele Identifier: CA435181942
Gene: NECTIN3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.110841074T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.111122227T>C , CM000665.2:g.111122227T>C GRCh38
NC_000003.11:g.110841074T>C , CM000665.1:g.110841074T>C GRCh37
NC_000003.10:g.112323764T>C NCBI36
NG_029835.1:g.55469T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000485303.6:c.906T>C MANE Select ENSP00000418070.1:p.Ser302=
ENST00000319792.7:c.906T>C ENSP00000321514.3:p.Ser302=
ENST00000485303.5:c.906T>C ENSP00000418070.1:p.Ser302=
ENST00000486596.5:c.607T>C
ENST00000493615.5:c.837T>C ENSP00000420579.1:p.Ser279=
NM_001243286.1:c.906T>C NP_001230215.1:p.Ser302=
NM_001243288.1:c.837T>C NP_001230217.1:p.Ser279=
NM_015480.2:c.906T>C NP_056295.1:p.Ser302=
XM_005247322.3:c.906T>C XP_005247379.2:p.Ser302=
XM_011512662.1:c.999T>C XP_011510964.1:p.Ser333=
XM_011512663.1:c.999T>C XP_011510965.1:p.Ser333=
XM_011512664.1:c.837T>C XP_011510966.1:p.Ser279=
XM_011512665.1:c.999T>C XP_011510967.1:p.Ser333=
XM_011512666.1:c.999T>C XP_011510968.1:p.Ser333=
XM_011512667.1:c.270T>C XP_011510969.1:p.Ser90=
XR_924122.1:n.1229T>C
XM_017006123.1:c.999T>C XP_016861612.1:p.Ser333=
XM_017006124.1:c.861T>C XP_016861613.1:p.Ser287=
XM_017006125.1:c.837T>C XP_016861614.1:p.Ser279=
XM_017006126.1:c.906T>C XP_016861615.1:p.Ser302=
XM_017006127.2:c.270T>C XP_016861616.1:p.Ser90=
XR_002959508.1:n.1187T>C
XR_924122.2:n.1229T>C
NM_015480.3:c.906T>C MANE Select NP_056295.1:p.Ser302=
NM_001243286.2:c.906T>C NP_001230215.1:p.Ser302=
NM_001243288.2:c.837T>C NP_001230217.1:p.Ser279=