Canonical Allele Identifier: CA1948007231

Gene: TH

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2167896A= , CM000673.2:g.2167896A=	GRCh38
NC_000011.9:g.2189126A= , CM000673.1:g.2189126A=	GRCh37
NC_000011.8:g.2145702A=	NCBI36
NG_008128.1:g.8910T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000360.4:c.614T= MANE Select	NP_000351.2:p.Leu205=
ENST00000352909.8:c.614T= MANE Select	ENSP00000325951.4:p.Leu205=
NM_000360.3:c.614T=	NP_000351.2:p.Leu205=
NM_199292.2:c.707T=	NP_954986.2:p.Leu236=
NM_199292.3:c.707T=	NP_954986.2:p.Leu236=
NM_199293.2:c.695T=	NP_954987.2:p.Leu232=
NM_199293.3:c.695T=	NP_954987.2:p.Leu232=
ENST00000324155.8:c.*303T=	ENSP00000325831.3:n.*303T=
ENST00000333684.9:c.614T=	ENSP00000328814.6:p.Leu205=
ENST00000352909.7:c.614T=	ENSP00000325951.3:p.Leu205=
ENST00000381168.7:c.*303T=	ENSP00000370560.3:n.*303T=
ENST00000381175.5:c.695T=	ENSP00000370567.1:p.Leu232=
ENST00000381178.5:c.707T=	ENSP00000370571.1:p.Leu236=
ENST00000412076.1:c.54T=
ENST00000416223.5:c.54T=
ENST00000469226.1:n.363T=
XM_011520335.1:c.626T=	XP_011518637.1:p.Leu209=
XM_011520335.2:c.626T=	XP_011518637.1:p.Leu209=