Canonical Allele Identifier: CA379126002

Gene: TH

Linked Data

• gnomAD v4: 11-2166518-G-C
• MyVariant Identifiers: chr11:g.2187748G>C (hg19) ; chr11:g.2166518G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2166518G>C , CM000673.2:g.2166518G>C	GRCh38
NC_000011.9:g.2187748G>C , CM000673.1:g.2187748G>C	GRCh37
NC_000011.8:g.2144324G>C	NCBI36
NG_008128.1:g.10288C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352909.8:c.1009C>G MANE Select	ENSP00000325951.4:p.Pro337Ala
ENST00000324155.8:c.*698C>G	ENSP00000325831.3:n.*698C>G
ENST00000333684.9:c.727C>G	ENSP00000328814.6:p.Pro243Ala
ENST00000352909.7:c.1009C>G	ENSP00000325951.3:p.Pro337Ala
ENST00000381168.7:c.*729C>G	ENSP00000370560.3:n.*729C>G
ENST00000381175.5:c.1090C>G	ENSP00000370567.1:p.Pro364Ala
ENST00000381178.5:c.1102C>G	ENSP00000370571.1:p.Pro368Ala
ENST00000412076.1:c.167C>G
ENST00000416223.5:c.303C>G
ENST00000461172.1:n.174C>G
ENST00000479437.5:n.558C>G
NM_000360.3:c.1009C>G	NP_000351.2:p.Pro337Ala
NM_199292.2:c.1102C>G	NP_954986.2:p.Pro368Ala
NM_199293.2:c.1090C>G	NP_954987.2:p.Pro364Ala
XM_011520335.1:c.1021C>G	XP_011518637.1:p.Pro341Ala
XM_011520335.2:c.1021C>G	XP_011518637.1:p.Pro341Ala
NM_000360.4:c.1009C>G MANE Select	NP_000351.2:p.Pro337Ala
NM_199292.3:c.1102C>G	NP_954986.2:p.Pro368Ala
NM_199293.3:c.1090C>G	NP_954987.2:p.Pro364Ala