Canonical Allele Identifier: CA1948005326

Gene: TH

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2166642G= , CM000673.2:g.2166642G=	GRCh38
NC_000011.9:g.2187872G= , CM000673.1:g.2187872G=	GRCh37
NC_000011.8:g.2144448G=	NCBI36
NG_008128.1:g.10164C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352909.8:c.968C= MANE Select	ENSP00000325951.4:p.Ser323=
ENST00000324155.8:c.*657C=	ENSP00000325831.3:n.*657C=
ENST00000333684.9:c.696-93C=	ENSP00000328814.6:n.696-93C=
ENST00000352909.7:c.968C=	ENSP00000325951.3:p.Ser323=
ENST00000381168.7:c.*688C=	ENSP00000370560.3:n.*688C=
ENST00000381175.5:c.1049C=	ENSP00000370567.1:p.Ser350=
ENST00000381178.5:c.1061C=	ENSP00000370571.1:p.Ser354=
ENST00000412076.1:c.136-93C=
ENST00000416223.5:c.262C=
ENST00000461172.1:n.133C=
ENST00000479437.5:n.517C=
NM_000360.3:c.968C=	NP_000351.2:p.Ser323=
NM_199292.2:c.1061C=	NP_954986.2:p.Ser354=
NM_199293.2:c.1049C=	NP_954987.2:p.Ser350=
XM_011520335.1:c.980C=	XP_011518637.1:p.Ser327=
XM_011520335.2:c.980C=	XP_011518637.1:p.Ser327=
NM_000360.4:c.968C= MANE Select	NP_000351.2:p.Ser323=
NM_199292.3:c.1061C=	NP_954986.2:p.Ser354=
NM_199293.3:c.1049C=	NP_954987.2:p.Ser350=