Canonical Allele Identifier: CA379127181
Gene: TH HGNC NCBI

Linked Data

gnomAD v4: 11-2167031-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2167031T>A , CM000673.2:g.2167031T>A GRCh38
NC_000011.9:g.2188261T>A , CM000673.1:g.2188261T>A GRCh37
NC_000011.8:g.2144837T>A NCBI36
NG_008128.1:g.9775A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000352909.8:c.697A>T MANE Select ENSP00000325951.4:p.Lys233Ter
ENST00000324155.8:c.*386A>T ENSP00000325831.3:n.*386A>T
ENST00000333684.9:c.695+404A>T ENSP00000328814.6:n.695+404A>T
ENST00000352909.7:c.697A>T ENSP00000325951.3:p.Lys233Ter
ENST00000381168.7:c.*417A>T ENSP00000370560.3:n.*417A>T
ENST00000381175.5:c.778A>T ENSP00000370567.1:p.Lys260Ter
ENST00000381178.5:c.790A>T ENSP00000370571.1:p.Lys264Ter
ENST00000412076.1:c.135+404A>T
ENST00000416223.5:c.136-263A>T
ENST00000469226.1:n.826A>T
ENST00000479437.5:n.246A>T
NM_000360.3:c.697A>T NP_000351.2:p.Lys233Ter
NM_199292.2:c.790A>T NP_954986.2:p.Lys264Ter
NM_199293.2:c.778A>T NP_954987.2:p.Lys260Ter
XM_011520335.1:c.709A>T XP_011518637.1:p.Lys237Ter
XM_011520335.2:c.709A>T XP_011518637.1:p.Lys237Ter
NM_000360.4:c.697A>T MANE Select NP_000351.2:p.Lys233Ter
NM_199292.3:c.790A>T NP_954986.2:p.Lys264Ter
NM_199293.3:c.778A>T NP_954987.2:p.Lys260Ter