Canonical Allele Identifier: CA1821104756
Gene: TG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.133133217C= , CM000670.2:g.133133217C= GRCh38
NC_000008.10:g.134145461C= , CM000670.1:g.134145461C= GRCh37
NC_000008.9:g.134214643C= NCBI36
NG_015832.1:g.271257C=

Transcript Alleles

HGVS Amino-acid change
ENST00000220616.9:c.7998-253C= MANE Select ENSP00000220616.4:n.7998-253C=
ENST00000220616.8:c.7998-253C= ENSP00000220616.4:n.7998-253C=
ENST00000519178.5:c.3364-253C=
ENST00000519543.5:c.2397-253C= ENSP00000430430.1:n.2397-253C=
ENST00000521107.1:c.210-253C= ENSP00000430161.1:n.210-253C=
ENST00000523756.5:c.4653-253C=
NM_003235.4:c.7998-253C= NP_003226.4:n.7998-253C=
XM_005251038.3:c.7806-253C= XP_005251095.1:n.7806-253C=
XM_006716622.2:c.7935-253C= XP_006716685.1:n.7935-253C=
XM_005251038.4:c.7806-253C= XP_005251095.1:n.7806-253C=
XM_006716622.3:c.7935-253C= XP_006716685.1:n.7935-253C=
XM_017013793.1:c.7932-253C= XP_016869282.1:n.7932-253C=
XM_017013794.1:c.7863-253C= XP_016869283.1:n.7863-253C=
XM_017013795.1:c.7827-253C= XP_016869284.1:n.7827-253C=
XM_017013796.1:c.7779-253C= XP_016869285.1:n.7779-253C=
XM_017013797.1:c.7737-253C= XP_016869286.1:n.7737-253C=
NM_003235.5:c.7998-253C= MANE Select NP_003226.4:n.7998-253C=