Canonical Allele Identifier: CA1256215
Gene: TNR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.175406401G>T , CM000663.2:g.175406401G>T GRCh38
NC_000001.10:g.175375537G>T , CM000663.1:g.175375537G>T GRCh37
NC_000001.9:g.173642160G>T NCBI36
NG_050931.1:g.342302C>A

Transcript Alleles

HGVS Amino-acid Change
NM_003285.3:c.314C>A MANE Select NP_003276.3:p.Thr105Asn
ENST00000367674.7:c.314C>A MANE Select ENSP00000356646.1:p.Thr105Asn
NM_001328635.1:c.-582C>A NP_001315564.1:n.-582C>A
NM_001328635.2:c.-582C>A NP_001315564.1:n.-582C>A
NM_003285.2:c.314C>A NP_003276.3:p.Thr105Asn
ENST00000263525.6:c.314C>A ENSP00000263525.2:p.Thr105Asn
ENST00000367674.6:c.314C>A ENSP00000356646.1:p.Thr105Asn
XM_011509947.1:c.314C>A XP_011508249.1:p.Thr105Asn
XM_011509948.1:c.314C>A XP_011508250.1:p.Thr105Asn
XM_011509949.1:c.314C>A XP_011508251.1:p.Thr105Asn
XM_011509949.2:c.314C>A XP_011508251.1:p.Thr105Asn
XM_017002218.1:c.314C>A XP_016857707.1:p.Thr105Asn
XM_017002219.1:c.314C>A XP_016857708.1:p.Thr105Asn