Canonical Allele Identifier: CA379127136

Gene: TH

Linked Data

• MyVariant Identifiers: chr11:g.2188254A>T (hg19) ; chr11:g.2167024A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2167024A>T , CM000673.2:g.2167024A>T	GRCh38
NC_000011.9:g.2188254A>T , CM000673.1:g.2188254A>T	GRCh37
NC_000011.8:g.2144830A>T	NCBI36
NG_008128.1:g.9782T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352909.8:c.704T>A MANE Select	ENSP00000325951.4:p.Val235Asp
ENST00000324155.8:c.*393T>A	ENSP00000325831.3:n.*393T>A
ENST00000333684.9:c.695+411T>A	ENSP00000328814.6:n.695+411T>A
ENST00000352909.7:c.704T>A	ENSP00000325951.3:p.Val235Asp
ENST00000381168.7:c.*424T>A	ENSP00000370560.3:n.*424T>A
ENST00000381175.5:c.785T>A	ENSP00000370567.1:p.Val262Asp
ENST00000381178.5:c.797T>A	ENSP00000370571.1:p.Val266Asp
ENST00000412076.1:c.135+411T>A
ENST00000416223.5:c.136-256T>A
ENST00000469226.1:n.833T>A
ENST00000479437.5:n.253T>A
NM_000360.3:c.704T>A	NP_000351.2:p.Val235Asp
NM_199292.2:c.797T>A	NP_954986.2:p.Val266Asp
NM_199293.2:c.785T>A	NP_954987.2:p.Val262Asp
XM_011520335.1:c.716T>A	XP_011518637.1:p.Val239Asp
XM_011520335.2:c.716T>A	XP_011518637.1:p.Val239Asp
NM_000360.4:c.704T>A MANE Select	NP_000351.2:p.Val235Asp
NM_199292.3:c.797T>A	NP_954986.2:p.Val266Asp
NM_199293.3:c.785T>A	NP_954987.2:p.Val262Asp