Canonical Allele Identifier: CA1948009768

Gene: TH

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2169847G= , CM000673.2:g.2169847G=	GRCh38
NC_000011.9:g.2191077G= , CM000673.1:g.2191077G=	GRCh37
NC_000011.8:g.2147653G=	NCBI36
NG_008128.1:g.6959C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352909.8:c.115C= MANE Select	ENSP00000325951.4:p.Gln39=
ENST00000324155.8:c.91-152C=	ENSP00000325831.3:n.91-152C=
ENST00000333684.9:c.115C=	ENSP00000328814.6:p.Gln39=
ENST00000352909.7:c.115C=	ENSP00000325951.3:p.Gln39=
ENST00000381168.7:c.103-152C=	ENSP00000370560.3:n.103-152C=
ENST00000381175.5:c.196C=	ENSP00000370567.1:p.Gln66=
ENST00000381178.5:c.208C=	ENSP00000370571.1:p.Gln70=
NM_000360.3:c.115C=	NP_000351.2:p.Gln39=
NM_199292.2:c.208C=	NP_954986.2:p.Gln70=
NM_199293.2:c.196C=	NP_954987.2:p.Gln66=
XM_011520335.1:c.127C=	XP_011518637.1:p.Gln43=
XM_011520335.2:c.127C=	XP_011518637.1:p.Gln43=
NM_000360.4:c.115C= MANE Select	NP_000351.2:p.Gln39=
NM_199292.3:c.208C=	NP_954986.2:p.Gln70=
NM_199293.3:c.196C=	NP_954987.2:p.Gln66=