Canonical Allele Identifier: CA2611979298

Gene: TH

Linked Data

• gnomAD v4: 11-2169597-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2169597C>T , CM000673.2:g.2169597C>T	GRCh38
NC_000011.9:g.2190827C>T , CM000673.1:g.2190827C>T	GRCh37
NC_000011.8:g.2147403C>T	NCBI36
NG_008128.1:g.7209G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000352909.8:c.312+53G>A MANE Select	ENSP00000325951.4:n.312+53G>A
ENST00000324155.8:c.*1+53G>A	ENSP00000325831.3:n.*1+53G>A
ENST00000333684.9:c.312+53G>A	ENSP00000328814.6:n.312+53G>A
ENST00000352909.7:c.312+53G>A	ENSP00000325951.3:n.312+53G>A
ENST00000381168.7:c.*1+53G>A	ENSP00000370560.3:n.*1+53G>A
ENST00000381175.5:c.393+53G>A	ENSP00000370567.1:n.393+53G>A
ENST00000381178.5:c.405+53G>A	ENSP00000370571.1:n.405+53G>A
NM_000360.3:c.312+53G>A	NP_000351.2:n.312+53G>A
NM_199292.2:c.405+53G>A	NP_954986.2:n.405+53G>A
NM_199293.2:c.393+53G>A	NP_954987.2:n.393+53G>A
XM_011520335.1:c.324+53G>A	XP_011518637.1:n.324+53G>A
XM_011520335.2:c.324+53G>A	XP_011518637.1:n.324+53G>A
NM_000360.4:c.312+53G>A MANE Select	NP_000351.2:n.312+53G>A
NM_199292.3:c.405+53G>A	NP_954986.2:n.405+53G>A
NM_199293.3:c.393+53G>A	NP_954987.2:n.393+53G>A