Canonical Allele Identifier: CA1948005417
Gene: TH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2166701C= , CM000673.2:g.2166701C= GRCh38
NC_000011.9:g.2187931C= , CM000673.1:g.2187931C= GRCh37
NC_000011.8:g.2144507C= NCBI36
NG_008128.1:g.10105G=

Transcript Alleles

HGVS Amino-acid change
ENST00000352909.8:c.909G= MANE Select ENSP00000325951.4:p.Leu303=
ENST00000324155.8:c.*598G= ENSP00000325831.3:n.*598G=
ENST00000333684.9:c.696-152G= ENSP00000328814.6:n.696-152G=
ENST00000352909.7:c.909G= ENSP00000325951.3:p.Leu303=
ENST00000381168.7:c.*629G= ENSP00000370560.3:n.*629G=
ENST00000381175.5:c.990G= ENSP00000370567.1:p.Leu330=
ENST00000381178.5:c.1002G= ENSP00000370571.1:p.Leu334=
ENST00000412076.1:c.136-152G=
ENST00000416223.5:c.203G=
ENST00000461172.1:n.74G=
ENST00000479437.5:n.458G=
NM_000360.3:c.909G= NP_000351.2:p.Leu303=
NM_199292.2:c.1002G= NP_954986.2:p.Leu334=
NM_199293.2:c.990G= NP_954987.2:p.Leu330=
XM_011520335.1:c.921G= XP_011518637.1:p.Leu307=
XM_011520335.2:c.921G= XP_011518637.1:p.Leu307=
NM_000360.4:c.909G= MANE Select NP_000351.2:p.Leu303=
NM_199292.3:c.1002G= NP_954986.2:p.Leu334=
NM_199293.3:c.990G= NP_954987.2:p.Leu330=