Canonical Allele Identifier: CA2528516686
Gene: CACNB2 HGNC NCBI
NSUN6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.18539638del , CM000672.2:g.18539638del GRCh38
NC_000010.10:g.18828567del , CM000672.1:g.18828567del GRCh37
NC_000010.9:g.18868573del NCBI36
NG_016195.1:g.403962del

Transcript Alleles

HGVS Amino-acid Change
ENST00000377315.6:c.1753del (CACNB2) ENSP00000366532.4:p.Arg585AlafsTer9
ENST00000377319.9:c.1618del (CACNB2) ENSP00000366536.3:p.Arg540AlafsTer9
ENST00000645287.2:c.1741del (CACNB2) ENSP00000496203.1:p.Arg581AlafsTer9
ENST00000282343.13:c.1813del (CACNB2) ENSP00000282343.8:p.Arg605AlafsTer9
ENST00000324631.13:c.1897del (CACNB2) MANE Select ENSP00000320025.8:p.Arg633AlafsTer9
ENST00000377315.5:c.1753del (CACNB2) ENSP00000366532.4:p.Arg585AlafsTer9
ENST00000377319.8:c.1618del (CACNB2) ENSP00000366536.3:p.Arg540AlafsTer9
ENST00000377329.10:c.1735del (CACNB2) MANE Plus Clinical ENSP00000366546.4:p.Arg579AlafsTer9
ENST00000377331.8:c.1522del (CACNB2) ENSP00000366548.4:p.Arg508AlafsTer9
ENST00000643096.2:c.1699del (CACNB2) ENSP00000494209.2:p.Arg567AlafsTer9
ENST00000645287.1:c.1741del (CACNB2) ENSP00000496203.1:p.Arg581AlafsTer9
ENST00000647168.2:c.*1038del (CACNB2) ENSP00000495854.2:n.*1038del
ENST00000650685.1:c.1639del (CACNB2) ENSP00000498460.1:p.Arg547AlafsTer9
ENST00000651330.1:c.*1171del (CACNB2) ENSP00000498457.1:n.*1171del
ENST00000651468.1:c.1454del (CACNB2) ENSP00000498352.1:n.1454del
ENST00000651928.1:c.*1136del (CACNB2) ENSP00000499177.1:n.*1136del
ENST00000652391.1:c.1717del (CACNB2) ENSP00000498938.1:p.Arg573AlafsTer9
ENST00000652478.1:c.*997del (CACNB2) ENSP00000498812.1:n.*997del
ENST00000282343.12:c.1813del (CACNB2) ENSP00000282343.8:p.Arg605AlafsTer9
ENST00000324631.11:c.1897del (CACNB2) ENSP00000320025.7:p.Arg633AlafsTer9
ENST00000352115.10:c.1825del (CACNB2) ENSP00000344474.6:p.Arg609AlafsTer9
ENST00000377315.4:c.1753del (CACNB2) ENSP00000366532.4:p.Arg585AlafsTer9
ENST00000377319.7:c.1618del (CACNB2) ENSP00000366536.3:p.Arg540AlafsTer9
ENST00000377328.5:c.1147del (CACNB2) ENSP00000366545.1:p.Arg383AlafsTer9
ENST00000377329.8:c.1735del (CACNB2) ENSP00000366546.4:p.Arg579AlafsTer9
ENST00000377331.6:c.1741del (CACNB2) ENSP00000366548.2:p.Arg581AlafsTer9
ENST00000396576.6:c.1732del (CACNB2) ENSP00000379821.2:p.Arg578AlafsTer9
ENST00000612134.4:c.1601del (CACNB2) ENSP00000480563.1:n.1601del
ENST00000612743.1:c.409del (CACNB2) ENSP00000478676.1:p.Arg137AlafsTer9
ENST00000615785.4:c.982del (CACNB2) ENSP00000480260.1:p.Arg328AlafsTer9
ENST00000617363.4:c.1660del (CACNB2) ENSP00000479756.1:p.Arg554AlafsTer9
NM_000724.3:c.1732del (CACNB2) NP_000715.2:p.Arg578AlafsTer9
NM_001167945.1:c.1699del (CACNB2) NP_001161417.1:p.Arg567AlafsTer9
NM_201570.2:c.1753del (CACNB2) NP_963864.1:p.Arg585AlafsTer9
NM_201571.3:c.1813del (CACNB2) NP_963865.2:p.Arg605AlafsTer9
NM_201572.3:c.1741del (CACNB2) NP_963866.2:p.Arg581AlafsTer9
NM_201590.2:c.1735del (CACNB2) NP_963884.2:p.Arg579AlafsTer9
NM_201593.2:c.1783del (CACNB2) NP_963887.2:p.Arg595AlafsTer9
NM_201596.2:c.1897del (CACNB2) NP_963890.2:p.Arg633AlafsTer9
NM_201597.2:c.1825del (CACNB2) NP_963891.1:p.Arg609AlafsTer9
XM_005252588.2:c.1639del (CACNB2) XP_005252645.1:p.Arg547AlafsTer9
XM_005252591.2:c.1057del (CACNB2) XP_005252648.1:p.Arg353AlafsTer9
XM_006717502.2:c.1717del (CACNB2) XP_006717565.1:p.Arg573AlafsTer9
XM_011519659.1:c.1663del (CACNB2) XP_011517961.1:p.Arg555AlafsTer9
XM_011519660.1:c.1618del (CACNB2) XP_011517962.1:p.Arg540AlafsTer9
NM_001330060.1:c.1618del (CACNB2) NP_001316989.1:p.Arg540AlafsTer9
XM_005252588.4:c.1639del (CACNB2) XP_005252645.1:p.Arg547AlafsTer9
XM_005252591.3:c.1057del (CACNB2) XP_005252648.1:p.Arg353AlafsTer9
XM_006717502.3:c.1717del (CACNB2) XP_006717565.1:p.Arg573AlafsTer9
XM_011519659.2:c.1663del (CACNB2) XP_011517961.1:p.Arg555AlafsTer9
XM_017016625.1:c.1057del (CACNB2) XP_016872114.1:p.Arg353AlafsTer9
XR_001747060.1:n.2423+2431del (NSUN6)
XR_001747198.1:n.2022del (CACNB2)
NM_000724.4:c.1732del (CACNB2) NP_000715.2:p.Arg578AlafsTer9
NM_001167945.2:c.1699del (CACNB2) NP_001161417.1:p.Arg567AlafsTer9
NM_001330060.2:c.1618del (CACNB2) NP_001316989.1:p.Arg540AlafsTer9
NM_201570.3:c.1753del (CACNB2) NP_963864.1:p.Arg585AlafsTer9
NM_201571.4:c.1813del (CACNB2) NP_963865.2:p.Arg605AlafsTer9
NM_201572.4:c.1741del (CACNB2) NP_963866.2:p.Arg581AlafsTer9
NM_201590.3:c.1735del (CACNB2) MANE Plus Clinical NP_963884.2:p.Arg579AlafsTer9
NM_201593.3:c.1783del (CACNB2) NP_963887.2:p.Arg595AlafsTer9
NM_201596.3:c.1897del (CACNB2) MANE Select NP_963890.2:p.Arg633AlafsTer9
NM_201597.3:c.1825del (CACNB2) NP_963891.1:p.Arg609AlafsTer9