Canonical Allele Identifier: CA1948006116

Gene: TH

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2167039G= , CM000673.2:g.2167039G=	GRCh38
NC_000011.9:g.2188269G= , CM000673.1:g.2188269G=	GRCh37
NC_000011.8:g.2144845G=	NCBI36
NG_008128.1:g.9767C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352909.8:c.696-7C= MANE Select	ENSP00000325951.4:n.696-7C=
ENST00000324155.8:c.*385-7C=	ENSP00000325831.3:n.*385-7C=
ENST00000333684.9:c.695+396C=	ENSP00000328814.6:n.695+396C=
ENST00000352909.7:c.696-7C=	ENSP00000325951.3:n.696-7C=
ENST00000381168.7:c.*416-7C=	ENSP00000370560.3:n.*416-7C=
ENST00000381175.5:c.777-7C=	ENSP00000370567.1:n.777-7C=
ENST00000381178.5:c.789-7C=	ENSP00000370571.1:n.789-7C=
ENST00000412076.1:c.135+396C=
ENST00000416223.5:c.136-271C=
ENST00000469226.1:n.825-7C=
ENST00000479437.5:n.238C=
NM_000360.3:c.696-7C=	NP_000351.2:n.696-7C=
NM_199292.2:c.789-7C=	NP_954986.2:n.789-7C=
NM_199293.2:c.777-7C=	NP_954987.2:n.777-7C=
XM_011520335.1:c.708-7C=	XP_011518637.1:n.708-7C=
XM_011520335.2:c.708-7C=	XP_011518637.1:n.708-7C=
NM_000360.4:c.696-7C= MANE Select	NP_000351.2:n.696-7C=
NM_199292.3:c.789-7C=	NP_954986.2:n.789-7C=
NM_199293.3:c.777-7C=	NP_954987.2:n.777-7C=