Canonical Allele Identifier: CA1821046512

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133018025T= , CM000670.2:g.133018025T=	GRCh38
NC_000008.10:g.134030270T= , CM000670.1:g.134030270T=	GRCh37
NC_000008.9:g.134099452T=	NCBI36
NG_015832.1:g.156066T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.6782+28T= MANE Select	ENSP00000220616.4:n.6782+28T=
ENST00000220616.8:c.6782+28T=	ENSP00000220616.4:n.6782+28T=
ENST00000518108.1:c.168+159T=
ENST00000519178.5:c.2148+28T=
ENST00000519543.5:c.1181+28T=	ENSP00000430430.1:n.1181+28T=
ENST00000523756.5:c.3437+28T=
NM_003235.4:c.6782+28T=	NP_003226.4:n.6782+28T=
XM_005251038.3:c.6590+28T=	XP_005251095.1:n.6590+28T=
XM_006716622.2:c.6719+28T=	XP_006716685.1:n.6719+28T=
XM_005251038.4:c.6590+28T=	XP_005251095.1:n.6590+28T=
XM_006716622.3:c.6719+28T=	XP_006716685.1:n.6719+28T=
XM_017013793.1:c.6716+28T=	XP_016869282.1:n.6716+28T=
XM_017013794.1:c.6782+28T=	XP_016869283.1:n.6782+28T=
XM_017013795.1:c.6611+28T=	XP_016869284.1:n.6611+28T=
XM_017013796.1:c.6563+28T=	XP_016869285.1:n.6563+28T=
XM_017013797.1:c.6521+28T=	XP_016869286.1:n.6521+28T=
XM_017013798.1:c.6782+28T=	XP_016869287.1:n.6782+28T=
NM_003235.5:c.6782+28T= MANE Select	NP_003226.4:n.6782+28T=