Canonical Allele Identifier: CA1948005414
Gene: TH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2166698G= , CM000673.2:g.2166698G= GRCh38
NC_000011.9:g.2187928G= , CM000673.1:g.2187928G= GRCh37
NC_000011.8:g.2144504G= NCBI36
NG_008128.1:g.10108C=

Transcript Alleles

HGVS Amino-acid change
ENST00000352909.8:c.912C= MANE Select ENSP00000325951.4:p.Ala304=
ENST00000324155.8:c.*601C= ENSP00000325831.3:n.*601C=
ENST00000333684.9:c.696-149C= ENSP00000328814.6:n.696-149C=
ENST00000352909.7:c.912C= ENSP00000325951.3:p.Ala304=
ENST00000381168.7:c.*632C= ENSP00000370560.3:n.*632C=
ENST00000381175.5:c.993C= ENSP00000370567.1:p.Ala331=
ENST00000381178.5:c.1005C= ENSP00000370571.1:p.Ala335=
ENST00000412076.1:c.136-149C=
ENST00000416223.5:c.206C=
ENST00000461172.1:n.77C=
ENST00000479437.5:n.461C=
NM_000360.3:c.912C= NP_000351.2:p.Ala304=
NM_199292.2:c.1005C= NP_954986.2:p.Ala335=
NM_199293.2:c.993C= NP_954987.2:p.Ala331=
XM_011520335.1:c.924C= XP_011518637.1:p.Ala308=
XM_011520335.2:c.924C= XP_011518637.1:p.Ala308=
NM_000360.4:c.912C= MANE Select NP_000351.2:p.Ala304=
NM_199292.3:c.1005C= NP_954986.2:p.Ala335=
NM_199293.3:c.993C= NP_954987.2:p.Ala331=