Canonical Allele Identifier: CA1948006051

Gene: TH

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2167005G= , CM000673.2:g.2167005G=	GRCh38
NC_000011.9:g.2188235G= , CM000673.1:g.2188235G=	GRCh37
NC_000011.8:g.2144811G=	NCBI36
NG_008128.1:g.9801C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352909.8:c.723C= MANE Select	ENSP00000325951.4:p.Gly241=
ENST00000324155.8:c.*412C=	ENSP00000325831.3:n.*412C=
ENST00000333684.9:c.695+430C=	ENSP00000328814.6:n.695+430C=
ENST00000352909.7:c.723C=	ENSP00000325951.3:p.Gly241=
ENST00000381168.7:c.*443C=	ENSP00000370560.3:n.*443C=
ENST00000381175.5:c.804C=	ENSP00000370567.1:p.Gly268=
ENST00000381178.5:c.816C=	ENSP00000370571.1:p.Gly272=
ENST00000412076.1:c.135+430C=
ENST00000416223.5:c.136-237C=
ENST00000469226.1:n.852C=
ENST00000479437.5:n.272C=
NM_000360.3:c.723C=	NP_000351.2:p.Gly241=
NM_199292.2:c.816C=	NP_954986.2:p.Gly272=
NM_199293.2:c.804C=	NP_954987.2:p.Gly268=
XM_011520335.1:c.735C=	XP_011518637.1:p.Gly245=
XM_011520335.2:c.735C=	XP_011518637.1:p.Gly245=
NM_000360.4:c.723C= MANE Select	NP_000351.2:p.Gly241=
NM_199292.3:c.816C=	NP_954986.2:p.Gly272=
NM_199293.3:c.804C=	NP_954987.2:p.Gly268=