Canonical Allele Identifier: CA1821104890

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133483C= , CM000670.2:g.133133483C=	GRCh38
NC_000008.10:g.134145727C= , CM000670.1:g.134145727C=	GRCh37
NC_000008.9:g.134214909C=	NCBI36
NG_015832.1:g.271523C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8011C= MANE Select	ENSP00000220616.4:p.Pro2671=
ENST00000220616.8:c.8011C=	ENSP00000220616.4:p.Pro2671=
ENST00000519178.5:c.3377C=
ENST00000519543.5:c.2410C=	ENSP00000430430.1:p.Pro804=
ENST00000521107.1:c.223C=	ENSP00000430161.1:p.Pro75=
ENST00000522691.1:n.97C=
ENST00000523756.5:c.4666C=
NM_003235.4:c.8011C=	NP_003226.4:p.Pro2671=
XM_005251038.3:c.7819C=	XP_005251095.1:p.Pro2607=
XM_006716622.2:c.7948C=	XP_006716685.1:p.Pro2650=
XM_005251038.4:c.7819C=	XP_005251095.1:p.Pro2607=
XM_006716622.3:c.7948C=	XP_006716685.1:p.Pro2650=
XM_017013793.1:c.7945C=	XP_016869282.1:p.Pro2649=
XM_017013794.1:c.7876C=	XP_016869283.1:p.Pro2626=
XM_017013795.1:c.7840C=	XP_016869284.1:p.Pro2614=
XM_017013796.1:c.7792C=	XP_016869285.1:p.Pro2598=
XM_017013797.1:c.7750C=	XP_016869286.1:p.Pro2584=
NM_003235.5:c.8011C= MANE Select	NP_003226.4:p.Pro2671=