Canonical Allele Identifier: CA379126307

Gene: TH

Linked Data

• MyVariant Identifiers: chr11:g.2187965C>T (hg19) ; chr11:g.2166735C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2166735C>T , CM000673.2:g.2166735C>T	GRCh38
NC_000011.9:g.2187965C>T , CM000673.1:g.2187965C>T	GRCh37
NC_000011.8:g.2144541C>T	NCBI36
NG_008128.1:g.10071G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352909.8:c.875G>A MANE Select	ENSP00000325951.4:p.Gly292Asp
ENST00000324155.8:c.*564G>A	ENSP00000325831.3:n.*564G>A
ENST00000333684.9:c.696-186G>A	ENSP00000328814.6:n.696-186G>A
ENST00000352909.7:c.875G>A	ENSP00000325951.3:p.Gly292Asp
ENST00000381168.7:c.*595G>A	ENSP00000370560.3:n.*595G>A
ENST00000381175.5:c.956G>A	ENSP00000370567.1:p.Gly319Asp
ENST00000381178.5:c.968G>A	ENSP00000370571.1:p.Gly323Asp
ENST00000412076.1:c.136-186G>A
ENST00000416223.5:c.169G>A
ENST00000461172.1:n.40G>A
ENST00000479437.5:n.424G>A
NM_000360.3:c.875G>A	NP_000351.2:p.Gly292Asp
NM_199292.2:c.968G>A	NP_954986.2:p.Gly323Asp
NM_199293.2:c.956G>A	NP_954987.2:p.Gly319Asp
XM_011520335.1:c.887G>A	XP_011518637.1:p.Gly296Asp
XM_011520335.2:c.887G>A	XP_011518637.1:p.Gly296Asp
NM_000360.4:c.875G>A MANE Select	NP_000351.2:p.Gly292Asp
NM_199292.3:c.968G>A	NP_954986.2:p.Gly323Asp
NM_199293.3:c.956G>A	NP_954987.2:p.Gly319Asp