Canonical Allele Identifier: CA379112134

Gene: TH

Linked Data

• MyVariant Identifiers: chr11:g.2190887A>T (hg19) ; chr11:g.2169657A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2169657A>T , CM000673.2:g.2169657A>T	GRCh38
NC_000011.9:g.2190887A>T , CM000673.1:g.2190887A>T	GRCh37
NC_000011.8:g.2147463A>T	NCBI36
NG_008128.1:g.7149T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000352909.8:c.305T>A MANE Select	ENSP00000325951.4:p.Val102Glu
ENST00000324155.8:c.129T>A	ENSP00000325831.3:p.Gly43=
ENST00000333684.9:c.305T>A	ENSP00000328814.6:p.Val102Glu
ENST00000352909.7:c.305T>A	ENSP00000325951.3:p.Val102Glu
ENST00000381168.7:c.141T>A	ENSP00000370560.3:p.Gly47=
ENST00000381175.5:c.386T>A	ENSP00000370567.1:p.Val129Glu
ENST00000381178.5:c.398T>A	ENSP00000370571.1:p.Val133Glu
NM_000360.3:c.305T>A	NP_000351.2:p.Val102Glu
NM_199292.2:c.398T>A	NP_954986.2:p.Val133Glu
NM_199293.2:c.386T>A	NP_954987.2:p.Val129Glu
XM_011520335.1:c.317T>A	XP_011518637.1:p.Val106Glu
XM_011520335.2:c.317T>A	XP_011518637.1:p.Val106Glu
NM_000360.4:c.305T>A MANE Select	NP_000351.2:p.Val102Glu
NM_199292.3:c.398T>A	NP_954986.2:p.Val133Glu
NM_199293.3:c.386T>A	NP_954987.2:p.Val129Glu