Canonical Allele Identifier: CA472414225

Gene: TH

Linked Data

• MyVariant Identifiers: chr11:g.2187985G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2166755G>A , CM000673.2:g.2166755G>A	GRCh38
NC_000011.9:g.2187985G>A , CM000673.1:g.2187985G>A	GRCh37
NC_000011.8:g.2144561G>A	NCBI36
NG_008128.1:g.10051C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352909.8:c.855C>T MANE Select	ENSP00000325951.4:p.Phe285=
ENST00000324155.8:c.*544C>T	ENSP00000325831.3:n.*544C>T
ENST00000333684.9:c.696-206C>T	ENSP00000328814.6:n.696-206C>T
ENST00000352909.7:c.855C>T	ENSP00000325951.3:p.Phe285=
ENST00000381168.7:c.*575C>T	ENSP00000370560.3:n.*575C>T
ENST00000381175.5:c.936C>T	ENSP00000370567.1:p.Phe312=
ENST00000381178.5:c.948C>T	ENSP00000370571.1:p.Phe316=
ENST00000412076.1:c.136-206C>T
ENST00000416223.5:c.149C>T
ENST00000461172.1:n.20C>T
ENST00000479437.5:n.404C>T
NM_000360.3:c.855C>T	NP_000351.2:p.Phe285=
NM_199292.2:c.948C>T	NP_954986.2:p.Phe316=
NM_199293.2:c.936C>T	NP_954987.2:p.Phe312=
XM_011520335.1:c.867C>T	XP_011518637.1:p.Phe289=
XM_011520335.2:c.867C>T	XP_011518637.1:p.Phe289=
NM_000360.4:c.855C>T MANE Select	NP_000351.2:p.Phe285=
NM_199292.3:c.948C>T	NP_954986.2:p.Phe316=
NM_199293.3:c.936C>T	NP_954987.2:p.Phe312=