Canonical Allele Identifier: CA1255844

Gene: TNR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.175386016C>T , CM000663.2:g.175386016C>T	GRCh38
NC_000001.10:g.175355152C>T , CM000663.1:g.175355152C>T	GRCh37
NC_000001.9:g.173621775C>T	NCBI36
NG_050931.1:g.362687G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_003285.3:c.1777+16G>A MANE Select	NP_003276.3:n.1777+16G>A
ENST00000367674.7:c.1777+16G>A MANE Select	ENSP00000356646.1:n.1777+16G>A
NM_001328635.1:c.778+16G>A	NP_001315564.1:n.778+16G>A
NM_001328635.2:c.778+16G>A	NP_001315564.1:n.778+16G>A
NM_003285.2:c.1777+16G>A	NP_003276.3:n.1777+16G>A
ENST00000263525.6:c.1777+16G>A	ENSP00000263525.2:n.1777+16G>A
ENST00000367674.6:c.1777+16G>A	ENSP00000356646.1:n.1777+16G>A
XM_011509947.1:c.1777+16G>A	XP_011508249.1:n.1777+16G>A
XM_011509948.1:c.1513+16G>A	XP_011508250.1:n.1513+16G>A
XM_011509949.1:c.1300+16G>A	XP_011508251.1:n.1300+16G>A
XM_011509949.2:c.1300+16G>A	XP_011508251.1:n.1300+16G>A
XM_017002218.1:c.1777+16G>A	XP_016857707.1:n.1777+16G>A
XM_017002219.1:c.1777+16G>A	XP_016857708.1:n.1777+16G>A