Canonical Allele Identifier: CA379112339

Gene: TH

Linked Data

• MyVariant Identifiers: chr11:g.2190993G>C (hg19) ; chr11:g.2169763G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2169763G>C , CM000673.2:g.2169763G>C	GRCh38
NC_000011.9:g.2190993G>C , CM000673.1:g.2190993G>C	GRCh37
NC_000011.8:g.2147569G>C	NCBI36
NG_008128.1:g.7043C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000352909.8:c.199C>G MANE Select	ENSP00000325951.4:p.Pro67Ala
ENST00000324155.8:c.91-68C>G	ENSP00000325831.3:n.91-68C>G
ENST00000333684.9:c.199C>G	ENSP00000328814.6:p.Pro67Ala
ENST00000352909.7:c.199C>G	ENSP00000325951.3:p.Pro67Ala
ENST00000381168.7:c.103-68C>G	ENSP00000370560.3:n.103-68C>G
ENST00000381175.5:c.280C>G	ENSP00000370567.1:p.Pro94Ala
ENST00000381178.5:c.292C>G	ENSP00000370571.1:p.Pro98Ala
NM_000360.3:c.199C>G	NP_000351.2:p.Pro67Ala
NM_199292.2:c.292C>G	NP_954986.2:p.Pro98Ala
NM_199293.2:c.280C>G	NP_954987.2:p.Pro94Ala
XM_011520335.1:c.211C>G	XP_011518637.1:p.Pro71Ala
XM_011520335.2:c.211C>G	XP_011518637.1:p.Pro71Ala
NM_000360.4:c.199C>G MANE Select	NP_000351.2:p.Pro67Ala
NM_199292.3:c.292C>G	NP_954986.2:p.Pro98Ala
NM_199293.3:c.280C>G	NP_954987.2:p.Pro94Ala