Canonical Allele Identifier: CA1948009777

Gene: TH

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2169853G= , CM000673.2:g.2169853G=	GRCh38
NC_000011.9:g.2191083G= , CM000673.1:g.2191083G=	GRCh37
NC_000011.8:g.2147659G=	NCBI36
NG_008128.1:g.6953C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352909.8:c.109C= MANE Select	ENSP00000325951.4:p.Arg37=
ENST00000324155.8:c.91-158C=	ENSP00000325831.3:n.91-158C=
ENST00000333684.9:c.109C=	ENSP00000328814.6:p.Arg37=
ENST00000352909.7:c.109C=	ENSP00000325951.3:p.Arg37=
ENST00000381168.7:c.103-158C=	ENSP00000370560.3:n.103-158C=
ENST00000381175.5:c.190C=	ENSP00000370567.1:p.Arg64=
ENST00000381178.5:c.202C=	ENSP00000370571.1:p.Arg68=
NM_000360.3:c.109C=	NP_000351.2:p.Arg37=
NM_199292.2:c.202C=	NP_954986.2:p.Arg68=
NM_199293.2:c.190C=	NP_954987.2:p.Arg64=
XM_011520335.1:c.121C=	XP_011518637.1:p.Arg41=
XM_011520335.2:c.121C=	XP_011518637.1:p.Arg41=
NM_000360.4:c.109C= MANE Select	NP_000351.2:p.Arg37=
NM_199292.3:c.202C=	NP_954986.2:p.Arg68=
NM_199293.3:c.190C=	NP_954987.2:p.Arg64=