Canonical Allele Identifier: CA10576195
Gene: TANC1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 225940
ClinVar RCV Id: RCV000211412
dbSNP Id: rs10497203

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.158994911A>C , CM000664.2:g.158994911A>C GRCh38
NC_000002.11:g.159851423A>C , CM000664.1:g.159851423A>C GRCh37
NC_000002.10:g.159559669A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001145909.1:c.-125-6169A>C VV NP_001139381.1:p.=
NM_033394.2:c.-125-6169A>C VV NP_203752.2:p.=
XM_006712810.2:c.-16+26129A>C XP_006712873.1:p.=
XM_006712812.2:c.-125-6169A>C XP_006712875.1:p.=
XM_011512048.1:c.-242-6169A>C XP_011510350.1:p.=
XM_011512051.1:c.-125-6169A>C XP_011510353.1:p.=
XM_011512053.1:c.-16+26129A>C XP_011510355.1:p.=
XM_011512055.1:c.-125-6169A>C XP_011510357.1:p.=
XM_011512058.1:c.-125-6169A>C XP_011510360.1:p.=
NM_001350062.1:c.-125-6169A>C VV NP_001336991.1:p.=
NM_001350063.1:c.-125-6169A>C VV NP_001336992.1:p.=
NM_001350064.1:c.-125-6169A>C VV NP_001336993.1:p.=
NM_001350065.1:c.-294-6169A>C VV NP_001336994.1:p.=
NR_146421.1:n.150-6169A>C
XM_006712810.3:c.-16+26129A>C
XM_006712812.3:c.-125-6169A>C
XM_011512048.2:c.-242-6169A>C
XM_011512051.2:c.-125-6169A>C
XM_011512053.2:c.-16+26129A>C
XM_011512055.2:c.-125-6169A>C
XM_011512058.2:c.-125-6169A>C
XM_017005142.1:c.-422-6169A>C XP_016860631.1:p.=
XM_017005145.1:c.-294-6169A>C XP_016860634.1:p.=
XM_017005146.1:c.-125-6169A>C XP_016860635.1:p.=
XM_017005154.1:c.-294-6169A>C XP_016860643.1:p.=
XR_002959352.1:n.142-6169A>C
XR_002959353.1:n.142-6169A>C
NM_033394.3:c.-125-6169A>C VV MANE Preferred
ENST00000263635.7:c.-125-6169A>C ENSP00000263635.6:p.=
ENST00000454300.5:c.-443-6169A>C ENSP00000396339.2:p.=