Canonical Allele Identifier: CA2611965389

Gene: TH

Linked Data

• gnomAD v4: 11-2167079-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2167079C>T , CM000673.2:g.2167079C>T	GRCh38
NC_000011.9:g.2188309C>T , CM000673.1:g.2188309C>T	GRCh37
NC_000011.8:g.2144885C>T	NCBI36
NG_008128.1:g.9727G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352909.8:c.696-47G>A MANE Select	ENSP00000325951.4:n.696-47G>A
ENST00000324155.8:c.*385-47G>A	ENSP00000325831.3:n.*385-47G>A
ENST00000333684.9:c.695+356G>A	ENSP00000328814.6:n.695+356G>A
ENST00000352909.7:c.696-47G>A	ENSP00000325951.3:n.696-47G>A
ENST00000381168.7:c.*416-47G>A	ENSP00000370560.3:n.*416-47G>A
ENST00000381175.5:c.777-47G>A	ENSP00000370567.1:n.777-47G>A
ENST00000381178.5:c.789-47G>A	ENSP00000370571.1:n.789-47G>A
ENST00000412076.1:c.135+356G>A
ENST00000416223.5:c.136-311G>A
ENST00000469226.1:n.825-47G>A
ENST00000479437.5:n.198G>A
NM_000360.3:c.696-47G>A	NP_000351.2:n.696-47G>A
NM_199292.2:c.789-47G>A	NP_954986.2:n.789-47G>A
NM_199293.2:c.777-47G>A	NP_954987.2:n.777-47G>A
XM_011520335.1:c.708-47G>A	XP_011518637.1:n.708-47G>A
XM_011520335.2:c.708-47G>A	XP_011518637.1:n.708-47G>A
NM_000360.4:c.696-47G>A MANE Select	NP_000351.2:n.696-47G>A
NM_199292.3:c.789-47G>A	NP_954986.2:n.789-47G>A
NM_199293.3:c.777-47G>A	NP_954987.2:n.777-47G>A