Canonical Allele Identifier: CA1948005756

Gene: TH

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2166888C= , CM000673.2:g.2166888C=	GRCh38
NC_000011.9:g.2188118C= , CM000673.1:g.2188118C=	GRCh37
NC_000011.8:g.2144694C=	NCBI36
NG_008128.1:g.9918G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352909.8:c.840G= MANE Select	ENSP00000325951.4:p.Lys280=
ENST00000324155.8:c.*529G=	ENSP00000325831.3:n.*529G=
ENST00000333684.9:c.696-339G=	ENSP00000328814.6:n.696-339G=
ENST00000352909.7:c.840G=	ENSP00000325951.3:p.Lys280=
ENST00000381168.7:c.*560G=	ENSP00000370560.3:n.*560G=
ENST00000381175.5:c.921G=	ENSP00000370567.1:p.Lys307=
ENST00000381178.5:c.933G=	ENSP00000370571.1:p.Lys311=
ENST00000412076.1:c.136-339G=
ENST00000416223.5:c.136-120G=
ENST00000479437.5:n.389G=
NM_000360.3:c.840G=	NP_000351.2:p.Lys280=
NM_199292.2:c.933G=	NP_954986.2:p.Lys311=
NM_199293.2:c.921G=	NP_954987.2:p.Lys307=
XM_011520335.1:c.852G=	XP_011518637.1:p.Lys284=
XM_011520335.2:c.852G=	XP_011518637.1:p.Lys284=
NM_000360.4:c.840G= MANE Select	NP_000351.2:p.Lys280=
NM_199292.3:c.933G=	NP_954986.2:p.Lys311=
NM_199293.3:c.921G=	NP_954987.2:p.Lys307=