Canonical Allele Identifier: CA1948005387

Gene: TH

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2166682A= , CM000673.2:g.2166682A=	GRCh38
NC_000011.9:g.2187912A= , CM000673.1:g.2187912A=	GRCh37
NC_000011.8:g.2144488A=	NCBI36
NG_008128.1:g.10124T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352909.8:c.928T= MANE Select	ENSP00000325951.4:p.Cys310=
ENST00000324155.8:c.*617T=	ENSP00000325831.3:n.*617T=
ENST00000333684.9:c.696-133T=	ENSP00000328814.6:n.696-133T=
ENST00000352909.7:c.928T=	ENSP00000325951.3:p.Cys310=
ENST00000381168.7:c.*648T=	ENSP00000370560.3:n.*648T=
ENST00000381175.5:c.1009T=	ENSP00000370567.1:p.Cys337=
ENST00000381178.5:c.1021T=	ENSP00000370571.1:p.Cys341=
ENST00000412076.1:c.136-133T=
ENST00000416223.5:c.222T=
ENST00000461172.1:n.93T=
ENST00000479437.5:n.477T=
NM_000360.3:c.928T=	NP_000351.2:p.Cys310=
NM_199292.2:c.1021T=	NP_954986.2:p.Cys341=
NM_199293.2:c.1009T=	NP_954987.2:p.Cys337=
XM_011520335.1:c.940T=	XP_011518637.1:p.Cys314=
XM_011520335.2:c.940T=	XP_011518637.1:p.Cys314=
NM_000360.4:c.928T= MANE Select	NP_000351.2:p.Cys310=
NM_199292.3:c.1021T=	NP_954986.2:p.Cys341=
NM_199293.3:c.1009T=	NP_954987.2:p.Cys337=