Canonical Allele Identifier: CA472414297

Gene: TH

Linked Data

• MyVariant Identifiers: chr11:g.2187994G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2166764G>A , CM000673.2:g.2166764G>A	GRCh38
NC_000011.9:g.2187994G>A , CM000673.1:g.2187994G>A	GRCh37
NC_000011.8:g.2144570G>A	NCBI36
NG_008128.1:g.10042C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352909.8:c.846C>T MANE Select	ENSP00000325951.4:p.Arg282=
ENST00000324155.8:c.*535C>T	ENSP00000325831.3:n.*535C>T
ENST00000333684.9:c.696-215C>T	ENSP00000328814.6:n.696-215C>T
ENST00000352909.7:c.846C>T	ENSP00000325951.3:p.Arg282=
ENST00000381168.7:c.*566C>T	ENSP00000370560.3:n.*566C>T
ENST00000381175.5:c.927C>T	ENSP00000370567.1:p.Arg309=
ENST00000381178.5:c.939C>T	ENSP00000370571.1:p.Arg313=
ENST00000412076.1:c.136-215C>T
ENST00000416223.5:c.140C>T
ENST00000461172.1:n.11C>T
ENST00000479437.5:n.395C>T
NM_000360.3:c.846C>T	NP_000351.2:p.Arg282=
NM_199292.2:c.939C>T	NP_954986.2:p.Arg313=
NM_199293.2:c.927C>T	NP_954987.2:p.Arg309=
XM_011520335.1:c.858C>T	XP_011518637.1:p.Arg286=
XM_011520335.2:c.858C>T	XP_011518637.1:p.Arg286=
NM_000360.4:c.846C>T MANE Select	NP_000351.2:p.Arg282=
NM_199292.3:c.939C>T	NP_954986.2:p.Arg313=
NM_199293.3:c.927C>T	NP_954987.2:p.Arg309=