Canonical Allele Identifier: CA379126883

Gene: TH

Linked Data

• dbSNP Id: rs1846112969
• gnomAD v4: 11-2166971-C-T
• MyVariant Identifiers: chr11:g.2188201C>T (hg19) ; chr11:g.2166971C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2166971C>T , CM000673.2:g.2166971C>T	GRCh38
NC_000011.9:g.2188201C>T , CM000673.1:g.2188201C>T	GRCh37
NC_000011.8:g.2144777C>T	NCBI36
NG_008128.1:g.9835G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352909.8:c.757G>A MANE Select	ENSP00000325951.4:p.Glu253Lys
ENST00000324155.8:c.*446G>A	ENSP00000325831.3:n.*446G>A
ENST00000333684.9:c.696-422G>A	ENSP00000328814.6:n.696-422G>A
ENST00000352909.7:c.757G>A	ENSP00000325951.3:p.Glu253Lys
ENST00000381168.7:c.*477G>A	ENSP00000370560.3:n.*477G>A
ENST00000381175.5:c.838G>A	ENSP00000370567.1:p.Glu280Lys
ENST00000381178.5:c.850G>A	ENSP00000370571.1:p.Glu284Lys
ENST00000412076.1:c.136-422G>A
ENST00000416223.5:c.136-203G>A
ENST00000469226.1:n.886G>A
ENST00000479437.5:n.306G>A
NM_000360.3:c.757G>A	NP_000351.2:p.Glu253Lys
NM_199292.2:c.850G>A	NP_954986.2:p.Glu284Lys
NM_199293.2:c.838G>A	NP_954987.2:p.Glu280Lys
XM_011520335.1:c.769G>A	XP_011518637.1:p.Glu257Lys
XM_011520335.2:c.769G>A	XP_011518637.1:p.Glu257Lys
NM_000360.4:c.757G>A MANE Select	NP_000351.2:p.Glu253Lys
NM_199292.3:c.850G>A	NP_954986.2:p.Glu284Lys
NM_199293.3:c.838G>A	NP_954987.2:p.Glu280Lys