Canonical Allele Identifier: CA379128169

Gene: TH

Linked Data

• MyVariant Identifiers: chr11:g.2189147A>G (hg19) ; chr11:g.2167917A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2167917A>G , CM000673.2:g.2167917A>G	GRCh38
NC_000011.9:g.2189147A>G , CM000673.1:g.2189147A>G	GRCh37
NC_000011.8:g.2145723A>G	NCBI36
NG_008128.1:g.8889T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352909.8:c.593T>C MANE Select	ENSP00000325951.4:p.Val198Ala
ENST00000324155.8:c.*282T>C	ENSP00000325831.3:n.*282T>C
ENST00000333684.9:c.593T>C	ENSP00000328814.6:p.Val198Ala
ENST00000352909.7:c.593T>C	ENSP00000325951.3:p.Val198Ala
ENST00000381168.7:c.*282T>C	ENSP00000370560.3:n.*282T>C
ENST00000381175.5:c.674T>C	ENSP00000370567.1:p.Val225Ala
ENST00000381178.5:c.686T>C	ENSP00000370571.1:p.Val229Ala
ENST00000412076.1:c.33T>C
ENST00000416223.5:c.33T>C
ENST00000469226.1:n.342T>C
NM_000360.3:c.593T>C	NP_000351.2:p.Val198Ala
NM_199292.2:c.686T>C	NP_954986.2:p.Val229Ala
NM_199293.2:c.674T>C	NP_954987.2:p.Val225Ala
XM_011520335.1:c.605T>C	XP_011518637.1:p.Val202Ala
XM_011520335.2:c.605T>C	XP_011518637.1:p.Val202Ala
NM_000360.4:c.593T>C MANE Select	NP_000351.2:p.Val198Ala
NM_199292.3:c.686T>C	NP_954986.2:p.Val229Ala
NM_199293.3:c.674T>C	NP_954987.2:p.Val225Ala