Canonical Allele Identifier: CA379126225

Gene: TH

Linked Data

• gnomAD v4: 11-2166695-G-T
• MyVariant Identifiers: chr11:g.2187925G>T (hg19) ; chr11:g.2166695G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2166695G>T , CM000673.2:g.2166695G>T	GRCh38
NC_000011.9:g.2187925G>T , CM000673.1:g.2187925G>T	GRCh37
NC_000011.8:g.2144501G>T	NCBI36
NG_008128.1:g.10111C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000352909.8:c.915C>A MANE Select	ENSP00000325951.4:p.Phe305Leu
ENST00000324155.8:c.*604C>A	ENSP00000325831.3:n.*604C>A
ENST00000333684.9:c.696-146C>A	ENSP00000328814.6:n.696-146C>A
ENST00000352909.7:c.915C>A	ENSP00000325951.3:p.Phe305Leu
ENST00000381168.7:c.*635C>A	ENSP00000370560.3:n.*635C>A
ENST00000381175.5:c.996C>A	ENSP00000370567.1:p.Phe332Leu
ENST00000381178.5:c.1008C>A	ENSP00000370571.1:p.Phe336Leu
ENST00000412076.1:c.136-146C>A
ENST00000416223.5:c.209C>A
ENST00000461172.1:n.80C>A
ENST00000479437.5:n.464C>A
NM_000360.3:c.915C>A	NP_000351.2:p.Phe305Leu
NM_199292.2:c.1008C>A	NP_954986.2:p.Phe336Leu
NM_199293.2:c.996C>A	NP_954987.2:p.Phe332Leu
XM_011520335.1:c.927C>A	XP_011518637.1:p.Phe309Leu
XM_011520335.2:c.927C>A	XP_011518637.1:p.Phe309Leu
NM_000360.4:c.915C>A MANE Select	NP_000351.2:p.Phe305Leu
NM_199292.3:c.1008C>A	NP_954986.2:p.Phe336Leu
NM_199293.3:c.996C>A	NP_954987.2:p.Phe332Leu