Canonical Allele Identifier: CA379126945

Gene: TH

Linked Data

• gnomAD v4: 11-2166984-G-T
• MyVariant Identifiers: chr11:g.2188214G>T (hg19) ; chr11:g.2166984G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2166984G>T , CM000673.2:g.2166984G>T	GRCh38
NC_000011.9:g.2188214G>T , CM000673.1:g.2188214G>T	GRCh37
NC_000011.8:g.2144790G>T	NCBI36
NG_008128.1:g.9822C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352909.8:c.744C>A MANE Select	ENSP00000325951.4:p.Cys248Ter
ENST00000324155.8:c.*433C>A	ENSP00000325831.3:n.*433C>A
ENST00000333684.9:c.696-435C>A	ENSP00000328814.6:n.696-435C>A
ENST00000352909.7:c.744C>A	ENSP00000325951.3:p.Cys248Ter
ENST00000381168.7:c.*464C>A	ENSP00000370560.3:n.*464C>A
ENST00000381175.5:c.825C>A	ENSP00000370567.1:p.Cys275Ter
ENST00000381178.5:c.837C>A	ENSP00000370571.1:p.Cys279Ter
ENST00000412076.1:c.136-435C>A
ENST00000416223.5:c.136-216C>A
ENST00000469226.1:n.873C>A
ENST00000479437.5:n.293C>A
NM_000360.3:c.744C>A	NP_000351.2:p.Cys248Ter
NM_199292.2:c.837C>A	NP_954986.2:p.Cys279Ter
NM_199293.2:c.825C>A	NP_954987.2:p.Cys275Ter
XM_011520335.1:c.756C>A	XP_011518637.1:p.Cys252Ter
XM_011520335.2:c.756C>A	XP_011518637.1:p.Cys252Ter
NM_000360.4:c.744C>A MANE Select	NP_000351.2:p.Cys248Ter
NM_199292.3:c.837C>A	NP_954986.2:p.Cys279Ter
NM_199293.3:c.825C>A	NP_954987.2:p.Cys275Ter