Canonical Allele Identifier: CA379127105

Gene: TH

Linked Data

• gnomAD v4: 11-2167018-G-A
• MyVariant Identifiers: chr11:g.2188248G>A (hg19) ; chr11:g.2167018G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2167018G>A , CM000673.2:g.2167018G>A	GRCh38
NC_000011.9:g.2188248G>A , CM000673.1:g.2188248G>A	GRCh37
NC_000011.8:g.2144824G>A	NCBI36
NG_008128.1:g.9788C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352909.8:c.710C>T MANE Select	ENSP00000325951.4:p.Thr237Ile
ENST00000324155.8:c.*399C>T	ENSP00000325831.3:n.*399C>T
ENST00000333684.9:c.695+417C>T	ENSP00000328814.6:n.695+417C>T
ENST00000352909.7:c.710C>T	ENSP00000325951.3:p.Thr237Ile
ENST00000381168.7:c.*430C>T	ENSP00000370560.3:n.*430C>T
ENST00000381175.5:c.791C>T	ENSP00000370567.1:p.Thr264Ile
ENST00000381178.5:c.803C>T	ENSP00000370571.1:p.Thr268Ile
ENST00000412076.1:c.135+417C>T
ENST00000416223.5:c.136-250C>T
ENST00000469226.1:n.839C>T
ENST00000479437.5:n.259C>T
NM_000360.3:c.710C>T	NP_000351.2:p.Thr237Ile
NM_199292.2:c.803C>T	NP_954986.2:p.Thr268Ile
NM_199293.2:c.791C>T	NP_954987.2:p.Thr264Ile
XM_011520335.1:c.722C>T	XP_011518637.1:p.Thr241Ile
XM_011520335.2:c.722C>T	XP_011518637.1:p.Thr241Ile
NM_000360.4:c.710C>T MANE Select	NP_000351.2:p.Thr237Ile
NM_199292.3:c.803C>T	NP_954986.2:p.Thr268Ile
NM_199293.3:c.791C>T	NP_954987.2:p.Thr264Ile