Canonical Allele Identifier: CA379126229

Gene: TH

Linked Data

• gnomAD v4: 11-2166697-A-G
• MyVariant Identifiers: chr11:g.2187927A>G (hg19) ; chr11:g.2166697A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2166697A>G , CM000673.2:g.2166697A>G	GRCh38
NC_000011.9:g.2187927A>G , CM000673.1:g.2187927A>G	GRCh37
NC_000011.8:g.2144503A>G	NCBI36
NG_008128.1:g.10109T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000352909.8:c.913T>C MANE Select	ENSP00000325951.4:p.Phe305Leu
ENST00000324155.8:c.*602T>C	ENSP00000325831.3:n.*602T>C
ENST00000333684.9:c.696-148T>C	ENSP00000328814.6:n.696-148T>C
ENST00000352909.7:c.913T>C	ENSP00000325951.3:p.Phe305Leu
ENST00000381168.7:c.*633T>C	ENSP00000370560.3:n.*633T>C
ENST00000381175.5:c.994T>C	ENSP00000370567.1:p.Phe332Leu
ENST00000381178.5:c.1006T>C	ENSP00000370571.1:p.Phe336Leu
ENST00000412076.1:c.136-148T>C
ENST00000416223.5:c.207T>C
ENST00000461172.1:n.78T>C
ENST00000479437.5:n.462T>C
NM_000360.3:c.913T>C	NP_000351.2:p.Phe305Leu
NM_199292.2:c.1006T>C	NP_954986.2:p.Phe336Leu
NM_199293.2:c.994T>C	NP_954987.2:p.Phe332Leu
XM_011520335.1:c.925T>C	XP_011518637.1:p.Phe309Leu
XM_011520335.2:c.925T>C	XP_011518637.1:p.Phe309Leu
NM_000360.4:c.913T>C MANE Select	NP_000351.2:p.Phe305Leu
NM_199292.3:c.1006T>C	NP_954986.2:p.Phe336Leu
NM_199293.3:c.994T>C	NP_954987.2:p.Phe332Leu