Canonical Allele Identifier: CA472413979

Gene: TH

Linked Data

• MyVariant Identifiers: chr11:g.2187868A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2166638A>C , CM000673.2:g.2166638A>C	GRCh38
NC_000011.9:g.2187868A>C , CM000673.1:g.2187868A>C	GRCh37
NC_000011.8:g.2144444A>C	NCBI36
NG_008128.1:g.10168T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000352909.8:c.972T>G MANE Select	ENSP00000325951.4:p.Pro324=
ENST00000324155.8:c.*661T>G	ENSP00000325831.3:n.*661T>G
ENST00000333684.9:c.696-89T>G	ENSP00000328814.6:n.696-89T>G
ENST00000352909.7:c.972T>G	ENSP00000325951.3:p.Pro324=
ENST00000381168.7:c.*692T>G	ENSP00000370560.3:n.*692T>G
ENST00000381175.5:c.1053T>G	ENSP00000370567.1:p.Pro351=
ENST00000381178.5:c.1065T>G	ENSP00000370571.1:p.Pro355=
ENST00000412076.1:c.136-89T>G
ENST00000416223.5:c.266T>G
ENST00000461172.1:n.137T>G
ENST00000479437.5:n.521T>G
NM_000360.3:c.972T>G	NP_000351.2:p.Pro324=
NM_199292.2:c.1065T>G	NP_954986.2:p.Pro355=
NM_199293.2:c.1053T>G	NP_954987.2:p.Pro351=
XM_011520335.1:c.984T>G	XP_011518637.1:p.Pro328=
XM_011520335.2:c.984T>G	XP_011518637.1:p.Pro328=
NM_000360.4:c.972T>G MANE Select	NP_000351.2:p.Pro324=
NM_199292.3:c.1065T>G	NP_954986.2:p.Pro355=
NM_199293.3:c.1053T>G	NP_954987.2:p.Pro351=