Canonical Allele Identifier: CA379112328

Gene: TH

Linked Data

• MyVariant Identifiers: chr11:g.2190986T>A (hg19) ; chr11:g.2169756T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2169756T>A , CM000673.2:g.2169756T>A	GRCh38
NC_000011.9:g.2190986T>A , CM000673.1:g.2190986T>A	GRCh37
NC_000011.8:g.2147562T>A	NCBI36
NG_008128.1:g.7050A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000352909.8:c.206A>T MANE Select	ENSP00000325951.4:p.Glu69Val
ENST00000324155.8:c.91-61A>T	ENSP00000325831.3:n.91-61A>T
ENST00000333684.9:c.206A>T	ENSP00000328814.6:p.Glu69Val
ENST00000352909.7:c.206A>T	ENSP00000325951.3:p.Glu69Val
ENST00000381168.7:c.103-61A>T	ENSP00000370560.3:n.103-61A>T
ENST00000381175.5:c.287A>T	ENSP00000370567.1:p.Glu96Val
ENST00000381178.5:c.299A>T	ENSP00000370571.1:p.Glu100Val
NM_000360.3:c.206A>T	NP_000351.2:p.Glu69Val
NM_199292.2:c.299A>T	NP_954986.2:p.Glu100Val
NM_199293.2:c.287A>T	NP_954987.2:p.Glu96Val
XM_011520335.1:c.218A>T	XP_011518637.1:p.Glu73Val
XM_011520335.2:c.218A>T	XP_011518637.1:p.Glu73Val
NM_000360.4:c.206A>T MANE Select	NP_000351.2:p.Glu69Val
NM_199292.3:c.299A>T	NP_954986.2:p.Glu100Val
NM_199293.3:c.287A>T	NP_954987.2:p.Glu96Val