Canonical Allele Identifier: CA379125049

Gene: TH

Linked Data

• MyVariant Identifiers: chr11:g.2186520T>G (hg19) ; chr11:g.2165290T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2165290T>G , CM000673.2:g.2165290T>G	GRCh38
NC_000011.9:g.2186520T>G , CM000673.1:g.2186520T>G	GRCh37
NC_000011.8:g.2143096T>G	NCBI36
NG_007114.1:g.905A>C
NG_008128.1:g.11516A>C
NG_050578.1:g.920A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000352909.8:c.1276A>C MANE Select	ENSP00000325951.4:p.Thr426Pro
ENST00000333684.9:c.994A>C	ENSP00000328814.6:p.Thr332Pro
ENST00000352909.7:c.1276A>C	ENSP00000325951.3:p.Thr426Pro
ENST00000381175.5:c.1357A>C	ENSP00000370567.1:p.Thr453Pro
ENST00000381178.5:c.1369A>C	ENSP00000370571.1:p.Thr457Pro
NM_000360.3:c.1276A>C	NP_000351.2:p.Thr426Pro
NM_199292.2:c.1369A>C	NP_954986.2:p.Thr457Pro
NM_199293.2:c.1357A>C	NP_954987.2:p.Thr453Pro
XM_011520335.1:c.1288A>C	XP_011518637.1:p.Thr430Pro
XM_011520335.2:c.1288A>C	XP_011518637.1:p.Thr430Pro
NM_000360.4:c.1276A>C MANE Select	NP_000351.2:p.Thr426Pro
NM_199292.3:c.1369A>C	NP_954986.2:p.Thr457Pro
NM_199293.3:c.1357A>C	NP_954987.2:p.Thr453Pro