Canonical Allele Identifier: CA379125992

Gene: TH

Linked Data

• gnomAD v4: 11-2166514-A-G
• MyVariant Identifiers: chr11:g.2187744A>G (hg19) ; chr11:g.2166514A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2166514A>G , CM000673.2:g.2166514A>G	GRCh38
NC_000011.9:g.2187744A>G , CM000673.1:g.2187744A>G	GRCh37
NC_000011.8:g.2144320A>G	NCBI36
NG_008128.1:g.10292T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352909.8:c.1013T>C MANE Select	ENSP00000325951.4:p.Met338Thr
ENST00000324155.8:c.*702T>C	ENSP00000325831.3:n.*702T>C
ENST00000333684.9:c.731T>C	ENSP00000328814.6:p.Met244Thr
ENST00000352909.7:c.1013T>C	ENSP00000325951.3:p.Met338Thr
ENST00000381168.7:c.*733T>C	ENSP00000370560.3:n.*733T>C
ENST00000381175.5:c.1094T>C	ENSP00000370567.1:p.Met365Thr
ENST00000381178.5:c.1106T>C	ENSP00000370571.1:p.Met369Thr
ENST00000412076.1:c.171T>C
ENST00000416223.5:c.307T>C
ENST00000461172.1:n.178T>C
ENST00000479437.5:n.562T>C
NM_000360.3:c.1013T>C	NP_000351.2:p.Met338Thr
NM_199292.2:c.1106T>C	NP_954986.2:p.Met369Thr
NM_199293.2:c.1094T>C	NP_954987.2:p.Met365Thr
XM_011520335.1:c.1025T>C	XP_011518637.1:p.Met342Thr
XM_011520335.2:c.1025T>C	XP_011518637.1:p.Met342Thr
NM_000360.4:c.1013T>C MANE Select	NP_000351.2:p.Met338Thr
NM_199292.3:c.1106T>C	NP_954986.2:p.Met369Thr
NM_199293.3:c.1094T>C	NP_954987.2:p.Met365Thr