Canonical Allele Identifier: CA379126660

Gene: TH

Linked Data

• MyVariant Identifiers: chr11:g.2188158T>A (hg19) ; chr11:g.2166928T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2166928T>A , CM000673.2:g.2166928T>A	GRCh38
NC_000011.9:g.2188158T>A , CM000673.1:g.2188158T>A	GRCh37
NC_000011.8:g.2144734T>A	NCBI36
NG_008128.1:g.9878A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352909.8:c.800A>T MANE Select	ENSP00000325951.4:p.Asp267Val
ENST00000324155.8:c.*489A>T	ENSP00000325831.3:n.*489A>T
ENST00000333684.9:c.696-379A>T	ENSP00000328814.6:n.696-379A>T
ENST00000352909.7:c.800A>T	ENSP00000325951.3:p.Asp267Val
ENST00000381168.7:c.*520A>T	ENSP00000370560.3:n.*520A>T
ENST00000381175.5:c.881A>T	ENSP00000370567.1:p.Asp294Val
ENST00000381178.5:c.893A>T	ENSP00000370571.1:p.Asp298Val
ENST00000412076.1:c.136-379A>T
ENST00000416223.5:c.136-160A>T
ENST00000469226.1:n.929A>T
ENST00000479437.5:n.349A>T
NM_000360.3:c.800A>T	NP_000351.2:p.Asp267Val
NM_199292.2:c.893A>T	NP_954986.2:p.Asp298Val
NM_199293.2:c.881A>T	NP_954987.2:p.Asp294Val
XM_011520335.1:c.812A>T	XP_011518637.1:p.Asp271Val
XM_011520335.2:c.812A>T	XP_011518637.1:p.Asp271Val
NM_000360.4:c.800A>T MANE Select	NP_000351.2:p.Asp267Val
NM_199292.3:c.893A>T	NP_954986.2:p.Asp298Val
NM_199293.3:c.881A>T	NP_954987.2:p.Asp294Val