Canonical Allele Identifier: CA400545532
Community Standard Title: NM_001394998.1(TANC2):c.5350C>T (p.Arg1784Ter)
Gene: TANC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63421080C>T , CM000679.2:g.63421080C>T GRCh38
NC_000017.10:g.61498441C>T , CM000679.1:g.61498441C>T GRCh37
NC_000017.9:g.58852173C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001394998.1:c.5350C>T MANE Select NP_001381927.1:p.Arg1784Ter
ENST00000689528.1:c.5350C>T MANE Select ENSP00000510600.1:p.Arg1784Ter
NM_025185.3:c.5098C>T NP_079461.2:p.Arg1700Ter
NM_025185.4:c.5098C>T NP_079461.2:p.Arg1700Ter
ENST00000389520.8:c.5128C>T ENSP00000374171.4:p.Arg1710Ter
ENST00000424789.6:c.5098C>T ENSP00000387593.2:p.Arg1700Ter
ENST00000583356.5:c.4783C>T
ENST00000613171.4:c.2428C>T ENSP00000478576.1:p.Arg810Ter
XM_005257203.3:c.5098C>T XP_005257260.1:p.Arg1700Ter
XM_005257203.4:c.5098C>T XP_005257260.1:p.Arg1700Ter
XM_006721806.2:c.5350C>T XP_006721869.1:p.Arg1784Ter
XM_006721806.3:c.5350C>T XP_006721869.1:p.Arg1784Ter
XM_006721807.2:c.5320C>T XP_006721870.1:p.Arg1774Ter
XM_006721807.3:c.5320C>T XP_006721870.1:p.Arg1774Ter
XM_006721811.2:c.*1019C>T XP_006721874.1:n.*1019C>T
XM_006721811.4:c.*1019C>T XP_006721874.1:n.*1019C>T
XM_011524597.1:c.5353C>T XP_011522899.1:p.Arg1785Ter
XM_011524597.2:c.5353C>T XP_011522899.1:p.Arg1785Ter
XM_011524598.1:c.5323C>T XP_011522900.1:p.Arg1775Ter
XM_011524598.2:c.5323C>T XP_011522900.1:p.Arg1775Ter
XM_011524599.1:c.5305C>T XP_011522901.1:p.Arg1769Ter
XM_011524600.1:c.5242C>T XP_011522902.1:p.Arg1748Ter
XM_011524600.2:c.5242C>T XP_011522902.1:p.Arg1748Ter
XM_011524601.1:c.5242C>T XP_011522903.1:p.Arg1748Ter
XM_011524601.2:c.5242C>T XP_011522903.1:p.Arg1748Ter
XM_011524602.1:c.5131C>T XP_011522904.1:p.Arg1711Ter
XM_011524602.2:c.5131C>T XP_011522904.1:p.Arg1711Ter
XM_011524603.1:c.4861C>T XP_011522905.1:p.Arg1621Ter
XM_011524604.1:c.2203C>T XP_011522906.1:p.Arg735Ter
XM_017024429.1:c.5272C>T XP_016879918.1:p.Arg1758Ter
XM_017024430.2:c.4861C>T XP_016879919.1:p.Arg1621Ter