Canonical Allele Identifier: CA472414374

Gene: TH

Linked Data

• gnomAD v4: 11-2167011-C-A
• MyVariant Identifiers: chr11:g.2188241C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2167011C>A , CM000673.2:g.2167011C>A	GRCh38
NC_000011.9:g.2188241C>A , CM000673.1:g.2188241C>A	GRCh37
NC_000011.8:g.2144817C>A	NCBI36
NG_008128.1:g.9795G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352909.8:c.717G>T MANE Select	ENSP00000325951.4:p.Leu239=
ENST00000324155.8:c.*406G>T	ENSP00000325831.3:n.*406G>T
ENST00000333684.9:c.695+424G>T	ENSP00000328814.6:n.695+424G>T
ENST00000352909.7:c.717G>T	ENSP00000325951.3:p.Leu239=
ENST00000381168.7:c.*437G>T	ENSP00000370560.3:n.*437G>T
ENST00000381175.5:c.798G>T	ENSP00000370567.1:p.Leu266=
ENST00000381178.5:c.810G>T	ENSP00000370571.1:p.Leu270=
ENST00000412076.1:c.135+424G>T
ENST00000416223.5:c.136-243G>T
ENST00000469226.1:n.846G>T
ENST00000479437.5:n.266G>T
NM_000360.3:c.717G>T	NP_000351.2:p.Leu239=
NM_199292.2:c.810G>T	NP_954986.2:p.Leu270=
NM_199293.2:c.798G>T	NP_954987.2:p.Leu266=
XM_011520335.1:c.729G>T	XP_011518637.1:p.Leu243=
XM_011520335.2:c.729G>T	XP_011518637.1:p.Leu243=
NM_000360.4:c.717G>T MANE Select	NP_000351.2:p.Leu239=
NM_199292.3:c.810G>T	NP_954986.2:p.Leu270=
NM_199293.3:c.798G>T	NP_954987.2:p.Leu266=