Canonical Allele Identifier: CA1255813

Gene: TNR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.175379714G>C , CM000663.2:g.175379714G>C	GRCh38
NC_000001.10:g.175348850G>C , CM000663.1:g.175348850G>C	GRCh37
NC_000001.9:g.173615473G>C	NCBI36
NG_050931.1:g.368989C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_003285.3:c.1801C>G MANE Select	NP_003276.3:p.Arg601Gly
ENST00000367674.7:c.1801C>G MANE Select	ENSP00000356646.1:p.Arg601Gly
NM_001328635.1:c.802C>G	NP_001315564.1:p.Arg268Gly
NM_001328635.2:c.802C>G	NP_001315564.1:p.Arg268Gly
NM_003285.2:c.1801C>G	NP_003276.3:p.Arg601Gly
ENST00000263525.6:c.1801C>G	ENSP00000263525.2:p.Arg601Gly
ENST00000367674.6:c.1801C>G	ENSP00000356646.1:p.Arg601Gly
XM_011509947.1:c.1801C>G	XP_011508249.1:p.Arg601Gly
XM_011509948.1:c.1537C>G	XP_011508250.1:p.Arg513Gly
XM_011509949.1:c.1324C>G	XP_011508251.1:p.Arg442Gly
XM_011509949.2:c.1324C>G	XP_011508251.1:p.Arg442Gly
XM_017002218.1:c.1801C>G	XP_016857707.1:p.Arg601Gly
XM_017002219.1:c.1801C>G	XP_016857708.1:p.Arg601Gly