Canonical Allele Identifier: CA1821104982

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133661G= , CM000670.2:g.133133661G=	GRCh38
NC_000008.10:g.134145905G= , CM000670.1:g.134145905G=	GRCh37
NC_000008.9:g.134215087G=	NCBI36
NG_015832.1:g.271701G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8188+1G= MANE Select	ENSP00000220616.4:n.8188+1G=
ENST00000220616.8:c.8188+1G=	ENSP00000220616.4:n.8188+1G=
ENST00000519178.5:c.3554+1G=
ENST00000519543.5:c.2587+1G=	ENSP00000430430.1:n.2587+1G=
ENST00000521107.1:c.400+1G=	ENSP00000430161.1:n.400+1G=
ENST00000522691.1:n.274+1G=
ENST00000523756.5:c.4843+1G=
NM_003235.4:c.8188+1G=	NP_003226.4:n.8188+1G=
XM_005251038.3:c.7996+1G=	XP_005251095.1:n.7996+1G=
XM_006716622.2:c.8125+1G=	XP_006716685.1:n.8125+1G=
XM_005251038.4:c.7996+1G=	XP_005251095.1:n.7996+1G=
XM_006716622.3:c.8125+1G=	XP_006716685.1:n.8125+1G=
XM_017013793.1:c.8122+1G=	XP_016869282.1:n.8122+1G=
XM_017013794.1:c.8053+1G=	XP_016869283.1:n.8053+1G=
XM_017013795.1:c.8017+1G=	XP_016869284.1:n.8017+1G=
XM_017013796.1:c.7969+1G=	XP_016869285.1:n.7969+1G=
XM_017013797.1:c.7927+1G=	XP_016869286.1:n.7927+1G=
NM_003235.5:c.8188+1G= MANE Select	NP_003226.4:n.8188+1G=