Canonical Allele Identifier: CA1948009811

Gene: TH

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2169869G= , CM000673.2:g.2169869G=	GRCh38
NC_000011.9:g.2191099G= , CM000673.1:g.2191099G=	GRCh37
NC_000011.8:g.2147675G=	NCBI36
NG_008128.1:g.6937C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352909.8:c.93C= MANE Select	ENSP00000325951.4:p.Ser31=
ENST00000324155.8:c.91-174C=	ENSP00000325831.3:n.91-174C=
ENST00000333684.9:c.93C=	ENSP00000328814.6:p.Ser31=
ENST00000352909.7:c.93C=	ENSP00000325951.3:p.Ser31=
ENST00000381168.7:c.103-174C=	ENSP00000370560.3:n.103-174C=
ENST00000381175.5:c.174C=	ENSP00000370567.1:p.Ser58=
ENST00000381178.5:c.186C=	ENSP00000370571.1:p.Ser62=
NM_000360.3:c.93C=	NP_000351.2:p.Ser31=
NM_199292.2:c.186C=	NP_954986.2:p.Ser62=
NM_199293.2:c.174C=	NP_954987.2:p.Ser58=
XM_011520335.1:c.105C=	XP_011518637.1:p.Ser35=
XM_011520335.2:c.105C=	XP_011518637.1:p.Ser35=
NM_000360.4:c.93C= MANE Select	NP_000351.2:p.Ser31=
NM_199292.3:c.186C=	NP_954986.2:p.Ser62=
NM_199293.3:c.174C=	NP_954987.2:p.Ser58=