Canonical Allele Identifier: CA1948005373

Gene: TH

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2166678G= , CM000673.2:g.2166678G=	GRCh38
NC_000011.9:g.2187908G= , CM000673.1:g.2187908G=	GRCh37
NC_000011.8:g.2144484G=	NCBI36
NG_008128.1:g.10128C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352909.8:c.932C= MANE Select	ENSP00000325951.4:p.Thr311=
ENST00000324155.8:c.*621C=	ENSP00000325831.3:n.*621C=
ENST00000333684.9:c.696-129C=	ENSP00000328814.6:n.696-129C=
ENST00000352909.7:c.932C=	ENSP00000325951.3:p.Thr311=
ENST00000381168.7:c.*652C=	ENSP00000370560.3:n.*652C=
ENST00000381175.5:c.1013C=	ENSP00000370567.1:p.Thr338=
ENST00000381178.5:c.1025C=	ENSP00000370571.1:p.Thr342=
ENST00000412076.1:c.136-129C=
ENST00000416223.5:c.226C=
ENST00000461172.1:n.97C=
ENST00000479437.5:n.481C=
NM_000360.3:c.932C=	NP_000351.2:p.Thr311=
NM_199292.2:c.1025C=	NP_954986.2:p.Thr342=
NM_199293.2:c.1013C=	NP_954987.2:p.Thr338=
XM_011520335.1:c.944C=	XP_011518637.1:p.Thr315=
XM_011520335.2:c.944C=	XP_011518637.1:p.Thr315=
NM_000360.4:c.932C= MANE Select	NP_000351.2:p.Thr311=
NM_199292.3:c.1025C=	NP_954986.2:p.Thr342=
NM_199293.3:c.1013C=	NP_954987.2:p.Thr338=