Canonical Allele Identifier: CA1948007241

Gene: TH

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2167909G= , CM000673.2:g.2167909G=	GRCh38
NC_000011.9:g.2189139G= , CM000673.1:g.2189139G=	GRCh37
NC_000011.8:g.2145715G=	NCBI36
NG_008128.1:g.8897C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000360.4:c.601C= MANE Select	NP_000351.2:p.Gln201=
ENST00000352909.8:c.601C= MANE Select	ENSP00000325951.4:p.Gln201=
NM_000360.3:c.601C=	NP_000351.2:p.Gln201=
NM_199292.2:c.694C=	NP_954986.2:p.Gln232=
NM_199292.3:c.694C=	NP_954986.2:p.Gln232=
NM_199293.2:c.682C=	NP_954987.2:p.Gln228=
NM_199293.3:c.682C=	NP_954987.2:p.Gln228=
ENST00000324155.8:c.*290C=	ENSP00000325831.3:n.*290C=
ENST00000333684.9:c.601C=	ENSP00000328814.6:p.Gln201=
ENST00000352909.7:c.601C=	ENSP00000325951.3:p.Gln201=
ENST00000381168.7:c.*290C=	ENSP00000370560.3:n.*290C=
ENST00000381175.5:c.682C=	ENSP00000370567.1:p.Gln228=
ENST00000381178.5:c.694C=	ENSP00000370571.1:p.Gln232=
ENST00000412076.1:c.41C=
ENST00000416223.5:c.41C=
ENST00000469226.1:n.350C=
XM_011520335.1:c.613C=	XP_011518637.1:p.Gln205=
XM_011520335.2:c.613C=	XP_011518637.1:p.Gln205=