Canonical Allele Identifier: CA1255582

Gene: TNR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.175363788G>A , CM000663.2:g.175363788G>A	GRCh38
NC_000001.10:g.175332924G>A , CM000663.1:g.175332924G>A	GRCh37
NC_000001.9:g.173599547G>A	NCBI36
NG_050931.1:g.384915C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_003285.3:c.2627C>T MANE Select	NP_003276.3:p.Thr876Ile
ENST00000367674.7:c.2627C>T MANE Select	ENSP00000356646.1:p.Thr876Ile
NM_001328635.1:c.1628C>T	NP_001315564.1:p.Thr543Ile
NM_001328635.2:c.1628C>T	NP_001315564.1:p.Thr543Ile
NM_003285.2:c.2627C>T	NP_003276.3:p.Thr876Ile
ENST00000263525.6:c.2627C>T	ENSP00000263525.2:p.Thr876Ile
ENST00000367674.6:c.2627C>T	ENSP00000356646.1:p.Thr876Ile
XM_011509947.1:c.2627C>T	XP_011508249.1:p.Thr876Ile
XM_011509948.1:c.2363C>T	XP_011508250.1:p.Thr788Ile
XM_011509949.1:c.2150C>T	XP_011508251.1:p.Thr717Ile
XM_011509949.2:c.2150C>T	XP_011508251.1:p.Thr717Ile
XM_017002218.1:c.2627C>T	XP_016857707.1:p.Thr876Ile
XM_017002219.1:c.2627C>T	XP_016857708.1:p.Thr876Ile