Canonical Allele Identifier: CA1301663094
Gene: TANC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.158994918T= , CM000664.2:g.158994918T= GRCh38
NC_000002.11:g.159851430T= , CM000664.1:g.159851430T= GRCh37
NC_000002.10:g.159559676T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000263635.8:c.-125-6162T= MANE Select ENSP00000263635.6:n.-125-6162T=
ENST00000263635.7:c.-125-6162T= ENSP00000263635.6:n.-125-6162T=
ENST00000454300.5:c.-443-6162T= ENSP00000396339.2:n.-443-6162T=
NM_001145909.1:c.-125-6162T= NP_001139381.1:n.-125-6162T=
NM_033394.2:c.-125-6162T= NP_203752.2:n.-125-6162T=
XM_006712810.2:c.-16+26136T= XP_006712873.1:n.-16+26136T=
XM_006712812.2:c.-125-6162T= XP_006712875.1:n.-125-6162T=
XM_011512048.1:c.-242-6162T= XP_011510350.1:n.-242-6162T=
XM_011512051.1:c.-125-6162T= XP_011510353.1:n.-125-6162T=
XM_011512053.1:c.-16+26136T= XP_011510355.1:n.-16+26136T=
XM_011512055.1:c.-125-6162T= XP_011510357.1:n.-125-6162T=
XM_011512058.1:c.-125-6162T= XP_011510360.1:n.-125-6162T=
NM_001350062.1:c.-125-6162T= NP_001336991.1:n.-125-6162T=
NM_001350063.1:c.-125-6162T= NP_001336992.1:n.-125-6162T=
NM_001350064.1:c.-125-6162T= NP_001336993.1:n.-125-6162T=
NM_001350065.1:c.-294-6162T= NP_001336994.1:n.-294-6162T=
NR_146421.1:n.150-6162T=
XM_006712810.3:c.-16+26136T= XP_006712873.1:n.-16+26136T=
XM_006712812.3:c.-125-6162T= XP_006712875.1:n.-125-6162T=
XM_011512048.2:c.-242-6162T= XP_011510350.1:n.-242-6162T=
XM_011512051.2:c.-125-6162T= XP_011510353.1:n.-125-6162T=
XM_011512053.2:c.-16+26136T= XP_011510355.1:n.-16+26136T=
XM_011512055.2:c.-125-6162T= XP_011510357.1:n.-125-6162T=
XM_011512058.2:c.-125-6162T= XP_011510360.1:n.-125-6162T=
XM_017005142.1:c.-422-6162T= XP_016860631.1:n.-422-6162T=
XM_017005145.1:c.-294-6162T= XP_016860634.1:n.-294-6162T=
XM_017005146.1:c.-125-6162T= XP_016860635.1:n.-125-6162T=
XM_017005154.1:c.-294-6162T= XP_016860643.1:n.-294-6162T=
XR_002959352.1:n.142-6162T=
XR_002959353.1:n.142-6162T=
NM_033394.3:c.-125-6162T= MANE Select NP_203752.2:n.-125-6162T=
NR_146421.2:n.144-6162T=
NM_001145909.2:c.-125-6162T= NP_001139381.1:n.-125-6162T=
NM_001350062.2:c.-125-6162T= NP_001336991.1:n.-125-6162T=
NM_001350063.2:c.-125-6162T= NP_001336992.1:n.-125-6162T=
NM_001350064.2:c.-125-6162T= NP_001336993.1:n.-125-6162T=
NM_001350065.2:c.-294-6162T= NP_001336994.1:n.-294-6162T=