Canonical Allele Identifier: CA379128093

Gene: TH

Linked Data

• MyVariant Identifiers: chr11:g.2189131C>G (hg19) ; chr11:g.2167901C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2167901C>G , CM000673.2:g.2167901C>G	GRCh38
NC_000011.9:g.2189131C>G , CM000673.1:g.2189131C>G	GRCh37
NC_000011.8:g.2145707C>G	NCBI36
NG_008128.1:g.8905G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000352909.8:c.609G>C MANE Select	ENSP00000325951.4:p.Arg203Ser
ENST00000324155.8:c.*298G>C	ENSP00000325831.3:n.*298G>C
ENST00000333684.9:c.609G>C	ENSP00000328814.6:p.Arg203Ser
ENST00000352909.7:c.609G>C	ENSP00000325951.3:p.Arg203Ser
ENST00000381168.7:c.*298G>C	ENSP00000370560.3:n.*298G>C
ENST00000381175.5:c.690G>C	ENSP00000370567.1:p.Arg230Ser
ENST00000381178.5:c.702G>C	ENSP00000370571.1:p.Arg234Ser
ENST00000412076.1:c.49G>C
ENST00000416223.5:c.49G>C
ENST00000469226.1:n.358G>C
NM_000360.3:c.609G>C	NP_000351.2:p.Arg203Ser
NM_199292.2:c.702G>C	NP_954986.2:p.Arg234Ser
NM_199293.2:c.690G>C	NP_954987.2:p.Arg230Ser
XM_011520335.1:c.621G>C	XP_011518637.1:p.Arg207Ser
XM_011520335.2:c.621G>C	XP_011518637.1:p.Arg207Ser
NM_000360.4:c.609G>C MANE Select	NP_000351.2:p.Arg203Ser
NM_199292.3:c.702G>C	NP_954986.2:p.Arg234Ser
NM_199293.3:c.690G>C	NP_954987.2:p.Arg230Ser