Canonical Allele Identifier: CA1948009784

Gene: TH

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2169855C= , CM000673.2:g.2169855C=	GRCh38
NC_000011.9:g.2191085C= , CM000673.1:g.2191085C=	GRCh37
NC_000011.8:g.2147661C=	NCBI36
NG_008128.1:g.6951G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000352909.8:c.107G= MANE Select	ENSP00000325951.4:p.Gly36=
ENST00000324155.8:c.91-160G=	ENSP00000325831.3:n.91-160G=
ENST00000333684.9:c.107G=	ENSP00000328814.6:p.Gly36=
ENST00000352909.7:c.107G=	ENSP00000325951.3:p.Gly36=
ENST00000381168.7:c.103-160G=	ENSP00000370560.3:n.103-160G=
ENST00000381175.5:c.188G=	ENSP00000370567.1:p.Gly63=
ENST00000381178.5:c.200G=	ENSP00000370571.1:p.Gly67=
NM_000360.3:c.107G=	NP_000351.2:p.Gly36=
NM_199292.2:c.200G=	NP_954986.2:p.Gly67=
NM_199293.2:c.188G=	NP_954987.2:p.Gly63=
XM_011520335.1:c.119G=	XP_011518637.1:p.Gly40=
XM_011520335.2:c.119G=	XP_011518637.1:p.Gly40=
NM_000360.4:c.107G= MANE Select	NP_000351.2:p.Gly36=
NM_199292.3:c.200G=	NP_954986.2:p.Gly67=
NM_199293.3:c.188G=	NP_954987.2:p.Gly63=