Canonical Allele Identifier: CA1208549445

Gene: TNR

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.175327312T>G , CM000663.2:g.175327312T>G	GRCh38
NC_000001.10:g.175296448T>G , CM000663.1:g.175296448T>G	GRCh37
NC_000001.9:g.173563071T>G	NCBI36
NG_050931.1:g.421391A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367674.7:c.3793+2762A>C MANE Select	ENSP00000356646.1:n.3793+2762A>C
ENST00000263525.6:c.3793+2762A>C	ENSP00000263525.2:n.3793+2762A>C
ENST00000367674.6:c.3793+2762A>C	ENSP00000356646.1:n.3793+2762A>C
NM_003285.2:c.3793+2762A>C	NP_003276.3:n.3793+2762A>C
XM_011509947.1:c.3793+2762A>C	XP_011508249.1:n.3793+2762A>C
XM_011509948.1:c.3529+2762A>C	XP_011508250.1:n.3529+2762A>C
XM_011509949.1:c.3316+2762A>C	XP_011508251.1:n.3316+2762A>C
NM_001328635.1:c.2794+2762A>C	NP_001315564.1:n.2794+2762A>C
XM_011509949.2:c.3316+2762A>C	XP_011508251.1:n.3316+2762A>C
XM_017002218.1:c.3793+2762A>C	XP_016857707.1:n.3793+2762A>C
XM_017002219.1:c.3793+2762A>C	XP_016857708.1:n.3793+2762A>C
XR_001738299.1:n.90-2112T>G
XR_001738300.1:n.90-2112T>G
XR_001738301.1:n.68-5996T>G
XR_001738302.1:n.79-6010T>G
XR_001738303.1:n.90-2112T>G
NM_003285.3:c.3793+2762A>C MANE Select	NP_003276.3:n.3793+2762A>C
NM_001328635.2:c.2794+2762A>C	NP_001315564.1:n.2794+2762A>C