Canonical Allele Identifier: CA372236822
Gene: TG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.132971857T>G , CM000670.2:g.132971857T>G GRCh38
NC_000008.10:g.133984102T>G , CM000670.1:g.133984102T>G GRCh37
NC_000008.9:g.134053284T>G NCBI36
NG_015832.1:g.109898T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000220616.9:c.6039T>G MANE Select ENSP00000220616.4:p.Asn2013Lys
ENST00000220616.8:c.6039T>G ENSP00000220616.4:p.Asn2013Lys
ENST00000519178.5:c.1405T>G
ENST00000519294.5:n.31T>G
ENST00000519543.5:c.501T>G ENSP00000430430.1:p.Asn167Lys
ENST00000520089.5:n.148T>G
ENST00000520197.5:n.176T>G
ENST00000523756.5:c.2694T>G
ENST00000524151.5:n.7T>G
NM_003235.4:c.6039T>G NP_003226.4:p.Asn2013Lys
XM_005251038.3:c.5847T>G XP_005251095.1:p.Asn1949Lys
XM_005251040.3:c.6039T>G XP_005251097.1:p.Asn2013Lys
XM_005251042.3:c.6039T>G XP_005251099.1:p.Asn2013Lys
XM_005251043.3:c.6039T>G XP_005251100.1:p.Asn2013Lys
XM_006716622.2:c.6039T>G XP_006716685.1:p.Asn2013Lys
XM_005251038.4:c.5847T>G XP_005251095.1:p.Asn1949Lys
XM_005251040.4:c.6039T>G XP_005251097.1:p.Asn2013Lys
XM_005251042.4:c.6039T>G XP_005251099.1:p.Asn2013Lys
XM_006716622.3:c.6039T>G XP_006716685.1:p.Asn2013Lys
XM_017013793.1:c.5973T>G XP_016869282.1:p.Asn1991Lys
XM_017013794.1:c.6039T>G XP_016869283.1:p.Asn2013Lys
XM_017013795.1:c.5868T>G XP_016869284.1:p.Asn1956Lys
XM_017013796.1:c.5820T>G XP_016869285.1:p.Asn1940Lys
XM_017013797.1:c.5778T>G XP_016869286.1:p.Asn1926Lys
XM_017013798.1:c.6039T>G XP_016869287.1:p.Asn2013Lys
XM_017013799.1:c.6039T>G XP_016869288.1:p.Asn2013Lys
XM_017013800.1:c.6039T>G XP_016869289.1:p.Asn2013Lys
NM_003235.5:c.6039T>G MANE Select NP_003226.4:p.Asn2013Lys