Canonical Allele Identifier: CA2611984265

Gene: TH

Linked Data

• gnomAD v4: 11-2171796-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2171798del , CM000673.2:g.2171798del	GRCh38
NC_000011.9:g.2193028del , CM000673.1:g.2193028del	GRCh37
NC_000011.8:g.2149604del	NCBI36
NG_008128.1:g.5009del

Transcript Alleles

HGVS	Amino-acid change
ENST00000352909.8:c.-11del MANE Select	ENSP00000325951.4:n.-11del
ENST00000324155.8:c.-11del	ENSP00000325831.3:n.-11del
ENST00000333684.9:c.-11del	ENSP00000328814.6:n.-11del
ENST00000352909.7:c.-11del	ENSP00000325951.3:n.-11del
ENST00000381168.7:c.-11del	ENSP00000370560.3:n.-11del
ENST00000381175.5:c.-11del	ENSP00000370567.1:n.-11del
ENST00000381178.5:c.-11del	ENSP00000370571.1:n.-11del
NM_000360.3:c.-11del	NP_000351.2:n.-11del
NM_199292.2:c.-11del	NP_954986.2:n.-11del
NM_199293.2:c.-11del	NP_954987.2:n.-11del
XM_011520335.1:c.-11del	XP_011518637.1:n.-11del
XM_011520335.2:c.-11del	XP_011518637.1:n.-11del
NM_000360.4:c.-11del MANE Select	NP_000351.2:n.-11del
NM_199292.3:c.-11del	NP_954986.2:n.-11del
NM_199293.3:c.-11del	NP_954987.2:n.-11del