Canonical Allele Identifier: CA1948005591

Gene: TH

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2166800C= , CM000673.2:g.2166800C=	GRCh38
NC_000011.9:g.2188030C= , CM000673.1:g.2188030C=	GRCh37
NC_000011.8:g.2144606C=	NCBI36
NG_008128.1:g.10006G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352909.8:c.842-32G= MANE Select	ENSP00000325951.4:n.842-32G=
ENST00000324155.8:c.*531-32G=	ENSP00000325831.3:n.*531-32G=
ENST00000333684.9:c.696-251G=	ENSP00000328814.6:n.696-251G=
ENST00000352909.7:c.842-32G=	ENSP00000325951.3:n.842-32G=
ENST00000381168.7:c.*562-32G=	ENSP00000370560.3:n.*562-32G=
ENST00000381175.5:c.923-32G=	ENSP00000370567.1:n.923-32G=
ENST00000381178.5:c.935-32G=	ENSP00000370571.1:n.935-32G=
ENST00000412076.1:c.136-251G=
ENST00000416223.5:c.136-32G=
ENST00000479437.5:n.391-32G=
NM_000360.3:c.842-32G=	NP_000351.2:n.842-32G=
NM_199292.2:c.935-32G=	NP_954986.2:n.935-32G=
NM_199293.2:c.923-32G=	NP_954987.2:n.923-32G=
XM_011520335.1:c.854-32G=	XP_011518637.1:n.854-32G=
XM_011520335.2:c.854-32G=	XP_011518637.1:n.854-32G=
NM_000360.4:c.842-32G= MANE Select	NP_000351.2:n.842-32G=
NM_199292.3:c.935-32G=	NP_954986.2:n.935-32G=
NM_199293.3:c.923-32G=	NP_954987.2:n.923-32G=