Canonical Allele Identifier: CA1948005406
Gene: TH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2166693C= , CM000673.2:g.2166693C= GRCh38
NC_000011.9:g.2187923C= , CM000673.1:g.2187923C= GRCh37
NC_000011.8:g.2144499C= NCBI36
NG_008128.1:g.10113G=

Transcript Alleles

HGVS Amino-acid change
ENST00000352909.8:c.917G= MANE Select ENSP00000325951.4:p.Arg306=
ENST00000324155.8:c.*606G= ENSP00000325831.3:n.*606G=
ENST00000333684.9:c.696-144G= ENSP00000328814.6:n.696-144G=
ENST00000352909.7:c.917G= ENSP00000325951.3:p.Arg306=
ENST00000381168.7:c.*637G= ENSP00000370560.3:n.*637G=
ENST00000381175.5:c.998G= ENSP00000370567.1:p.Arg333=
ENST00000381178.5:c.1010G= ENSP00000370571.1:p.Arg337=
ENST00000412076.1:c.136-144G=
ENST00000416223.5:c.211G=
ENST00000461172.1:n.82G=
ENST00000479437.5:n.466G=
NM_000360.3:c.917G= NP_000351.2:p.Arg306=
NM_199292.2:c.1010G= NP_954986.2:p.Arg337=
NM_199293.2:c.998G= NP_954987.2:p.Arg333=
XM_011520335.1:c.929G= XP_011518637.1:p.Arg310=
XM_011520335.2:c.929G= XP_011518637.1:p.Arg310=
NM_000360.4:c.917G= MANE Select NP_000351.2:p.Arg306=
NM_199292.3:c.1010G= NP_954986.2:p.Arg337=
NM_199293.3:c.998G= NP_954987.2:p.Arg333=