Canonical Allele Identifier: CA379126368

Gene: TH

Linked Data

• MyVariant Identifiers: chr11:g.2187982C>A (hg19) ; chr11:g.2166752C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2166752C>A , CM000673.2:g.2166752C>A	GRCh38
NC_000011.9:g.2187982C>A , CM000673.1:g.2187982C>A	GRCh37
NC_000011.8:g.2144558C>A	NCBI36
NG_008128.1:g.10054G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352909.8:c.858G>T MANE Select	ENSP00000325951.4:p.Gln286His
ENST00000324155.8:c.*547G>T	ENSP00000325831.3:n.*547G>T
ENST00000333684.9:c.696-203G>T	ENSP00000328814.6:n.696-203G>T
ENST00000352909.7:c.858G>T	ENSP00000325951.3:p.Gln286His
ENST00000381168.7:c.*578G>T	ENSP00000370560.3:n.*578G>T
ENST00000381175.5:c.939G>T	ENSP00000370567.1:p.Gln313His
ENST00000381178.5:c.951G>T	ENSP00000370571.1:p.Gln317His
ENST00000412076.1:c.136-203G>T
ENST00000416223.5:c.152G>T
ENST00000461172.1:n.23G>T
ENST00000479437.5:n.407G>T
NM_000360.3:c.858G>T	NP_000351.2:p.Gln286His
NM_199292.2:c.951G>T	NP_954986.2:p.Gln317His
NM_199293.2:c.939G>T	NP_954987.2:p.Gln313His
XM_011520335.1:c.870G>T	XP_011518637.1:p.Gln290His
XM_011520335.2:c.870G>T	XP_011518637.1:p.Gln290His
NM_000360.4:c.858G>T MANE Select	NP_000351.2:p.Gln286His
NM_199292.3:c.951G>T	NP_954986.2:p.Gln317His
NM_199293.3:c.939G>T	NP_954987.2:p.Gln313His