Canonical Allele Identifier: CA1948003275

Gene: TH

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2165113T= , CM000673.2:g.2165113T=	GRCh38
NC_000011.9:g.2186343T= , CM000673.1:g.2186343T=	GRCh37
NC_000011.8:g.2142919T=	NCBI36
NG_007114.1:g.1082A=
NG_008128.1:g.11693A=
NG_050578.1:g.1097A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000352909.8:c.1334+119A= MANE Select	ENSP00000325951.4:n.1334+119A=
ENST00000333684.9:c.1052+119A=	ENSP00000328814.6:n.1052+119A=
ENST00000352909.7:c.1334+119A=	ENSP00000325951.3:n.1334+119A=
ENST00000381175.5:c.1415+119A=	ENSP00000370567.1:n.1415+119A=
ENST00000381178.5:c.1427+119A=	ENSP00000370571.1:n.1427+119A=
NM_000360.3:c.1334+119A=	NP_000351.2:n.1334+119A=
NM_199292.2:c.1427+119A=	NP_954986.2:n.1427+119A=
NM_199293.2:c.1415+119A=	NP_954987.2:n.1415+119A=
XM_011520335.1:c.1346+119A=	XP_011518637.1:n.1346+119A=
XM_011520335.2:c.1346+119A=	XP_011518637.1:n.1346+119A=
NM_000360.4:c.1334+119A= MANE Select	NP_000351.2:n.1334+119A=
NM_199292.3:c.1427+119A=	NP_954986.2:n.1427+119A=
NM_199293.3:c.1415+119A=	NP_954987.2:n.1415+119A=