Canonical Allele Identifier: CA472035170

Gene: TH

Linked Data

• MyVariant Identifiers: chr11:g.2189149C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2167919C>T , CM000673.2:g.2167919C>T	GRCh38
NC_000011.9:g.2189149C>T , CM000673.1:g.2189149C>T	GRCh37
NC_000011.8:g.2145725C>T	NCBI36
NG_008128.1:g.8887G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000352909.8:c.591G>A MANE Select	ENSP00000325951.4:p.Gln197=
ENST00000324155.8:c.*280G>A	ENSP00000325831.3:n.*280G>A
ENST00000333684.9:c.591G>A	ENSP00000328814.6:p.Gln197=
ENST00000352909.7:c.591G>A	ENSP00000325951.3:p.Gln197=
ENST00000381168.7:c.*280G>A	ENSP00000370560.3:n.*280G>A
ENST00000381175.5:c.672G>A	ENSP00000370567.1:p.Gln224=
ENST00000381178.5:c.684G>A	ENSP00000370571.1:p.Gln228=
ENST00000412076.1:c.31G>A
ENST00000416223.5:c.31G>A
ENST00000469226.1:n.340G>A
NM_000360.3:c.591G>A	NP_000351.2:p.Gln197=
NM_199292.2:c.684G>A	NP_954986.2:p.Gln228=
NM_199293.2:c.672G>A	NP_954987.2:p.Gln224=
XM_011520335.1:c.603G>A	XP_011518637.1:p.Gln201=
XM_011520335.2:c.603G>A	XP_011518637.1:p.Gln201=
NM_000360.4:c.591G>A MANE Select	NP_000351.2:p.Gln197=
NM_199292.3:c.684G>A	NP_954986.2:p.Gln228=
NM_199293.3:c.672G>A	NP_954987.2:p.Gln224=