Canonical Allele Identifier: CA1948009491
Gene: TH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2169681G= , CM000673.2:g.2169681G= GRCh38
NC_000011.9:g.2190911G= , CM000673.1:g.2190911G= GRCh37
NC_000011.8:g.2147487G= NCBI36
NG_008128.1:g.7125C=

Transcript Alleles

HGVS Amino-acid change
ENST00000352909.8:c.281C= MANE Select ENSP00000325951.4:p.Ser94=
ENST00000324155.8:c.105C= ENSP00000325831.3:p.Leu35=
ENST00000333684.9:c.281C= ENSP00000328814.6:p.Ser94=
ENST00000352909.7:c.281C= ENSP00000325951.3:p.Ser94=
ENST00000381168.7:c.117C= ENSP00000370560.3:p.Leu39=
ENST00000381175.5:c.362C= ENSP00000370567.1:p.Ser121=
ENST00000381178.5:c.374C= ENSP00000370571.1:p.Ser125=
NM_000360.3:c.281C= NP_000351.2:p.Ser94=
NM_199292.2:c.374C= NP_954986.2:p.Ser125=
NM_199293.2:c.362C= NP_954987.2:p.Ser121=
XM_011520335.1:c.293C= XP_011518637.1:p.Ser98=
XM_011520335.2:c.293C= XP_011518637.1:p.Ser98=
NM_000360.4:c.281C= MANE Select NP_000351.2:p.Ser94=
NM_199292.3:c.374C= NP_954986.2:p.Ser125=
NM_199293.3:c.362C= NP_954987.2:p.Ser121=