Canonical Allele Identifier: CA379126023

Gene: TH

Linked Data

• MyVariant Identifiers: chr11:g.2187757C>A (hg19) ; chr11:g.2166527C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2166527C>A , CM000673.2:g.2166527C>A	GRCh38
NC_000011.9:g.2187757C>A , CM000673.1:g.2187757C>A	GRCh37
NC_000011.8:g.2144333C>A	NCBI36
NG_008128.1:g.10279G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352909.8:c.1000G>T MANE Select	ENSP00000325951.4:p.Gly334Trp
ENST00000324155.8:c.*689G>T	ENSP00000325831.3:n.*689G>T
ENST00000333684.9:c.718G>T	ENSP00000328814.6:p.Gly240Trp
ENST00000352909.7:c.1000G>T	ENSP00000325951.3:p.Gly334Trp
ENST00000381168.7:c.*720G>T	ENSP00000370560.3:n.*720G>T
ENST00000381175.5:c.1081G>T	ENSP00000370567.1:p.Gly361Trp
ENST00000381178.5:c.1093G>T	ENSP00000370571.1:p.Gly365Trp
ENST00000412076.1:c.158G>T
ENST00000416223.5:c.294G>T
ENST00000461172.1:n.165G>T
ENST00000479437.5:n.549G>T
NM_000360.3:c.1000G>T	NP_000351.2:p.Gly334Trp
NM_199292.2:c.1093G>T	NP_954986.2:p.Gly365Trp
NM_199293.2:c.1081G>T	NP_954987.2:p.Gly361Trp
XM_011520335.1:c.1012G>T	XP_011518637.1:p.Gly338Trp
XM_011520335.2:c.1012G>T	XP_011518637.1:p.Gly338Trp
NM_000360.4:c.1000G>T MANE Select	NP_000351.2:p.Gly334Trp
NM_199292.3:c.1093G>T	NP_954986.2:p.Gly365Trp
NM_199293.3:c.1081G>T	NP_954987.2:p.Gly361Trp