Canonical Allele Identifier: CA1948011928
Gene: TH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2171690C= , CM000673.2:g.2171690C= GRCh38
NC_000011.9:g.2192920C= , CM000673.1:g.2192920C= GRCh37
NC_000011.8:g.2149496C= NCBI36
NG_008128.1:g.5116G=

Transcript Alleles

HGVS Amino-acid change
ENST00000352909.8:c.90+7G= MANE Select ENSP00000325951.4:n.90+7G=
ENST00000324155.8:c.90+7G= ENSP00000325831.3:n.90+7G=
ENST00000333684.9:c.90+7G= ENSP00000328814.6:n.90+7G=
ENST00000352909.7:c.90+7G= ENSP00000325951.3:n.90+7G=
ENST00000381168.7:c.97G= ENSP00000370560.3:p.Gly33=
ENST00000381175.5:c.90+7G= ENSP00000370567.1:n.90+7G=
ENST00000381178.5:c.97G= ENSP00000370571.1:p.Gly33=
NM_000360.3:c.90+7G= NP_000351.2:n.90+7G=
NM_199292.2:c.97G= NP_954986.2:p.Gly33=
NM_199293.2:c.90+7G= NP_954987.2:n.90+7G=
XM_011520335.1:c.97G= XP_011518637.1:p.Gly33=
XM_011520335.2:c.97G= XP_011518637.1:p.Gly33=
NM_000360.4:c.90+7G= MANE Select NP_000351.2:n.90+7G=
NM_199292.3:c.97G= NP_954986.2:p.Gly33=
NM_199293.3:c.90+7G= NP_954987.2:n.90+7G=