Canonical Allele Identifier: CA343790569

Gene: TNR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.175403373C>T , CM000663.2:g.175403373C>T	GRCh38
NC_000001.10:g.175372509C>T , CM000663.1:g.175372509C>T	GRCh37
NC_000001.9:g.173639132C>T	NCBI36
NG_050931.1:g.345330G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367674.7:c.743G>A MANE Select	ENSP00000356646.1:p.Gly248Glu
ENST00000263525.6:c.743G>A	ENSP00000263525.2:p.Gly248Glu
ENST00000367674.6:c.743G>A	ENSP00000356646.1:p.Gly248Glu
ENST00000422274.2:c.149+2843G>A
NM_003285.2:c.743G>A	NP_003276.3:p.Gly248Glu
XM_011509947.1:c.743G>A	XP_011508249.1:p.Gly248Glu
XM_011509948.1:c.743G>A	XP_011508250.1:p.Gly248Glu
XM_011509949.1:c.499+2843G>A	XP_011508251.1:n.499+2843G>A
NM_001328635.1:c.-153G>A	NP_001315564.1:n.-153G>A
XM_011509949.2:c.499+2843G>A	XP_011508251.1:n.499+2843G>A
XM_017002218.1:c.743G>A	XP_016857707.1:p.Gly248Glu
XM_017002219.1:c.743G>A	XP_016857708.1:p.Gly248Glu
NM_003285.3:c.743G>A MANE Select	NP_003276.3:p.Gly248Glu
NM_001328635.2:c.-153G>A	NP_001315564.1:n.-153G>A