Canonical Allele Identifier: CA2611962479

Gene: TH

Linked Data

• gnomAD v4: 11-2166616-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2166616C>A , CM000673.2:g.2166616C>A	GRCh38
NC_000011.9:g.2187846C>A , CM000673.1:g.2187846C>A	GRCh37
NC_000011.8:g.2144422C>A	NCBI36
NG_008128.1:g.10190G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352909.8:c.977+17G>T MANE Select	ENSP00000325951.4:n.977+17G>T
ENST00000324155.8:c.*666+17G>T	ENSP00000325831.3:n.*666+17G>T
ENST00000333684.9:c.696-67G>T	ENSP00000328814.6:n.696-67G>T
ENST00000352909.7:c.977+17G>T	ENSP00000325951.3:n.977+17G>T
ENST00000381168.7:c.*697+17G>T	ENSP00000370560.3:n.*697+17G>T
ENST00000381175.5:c.1058+17G>T	ENSP00000370567.1:n.1058+17G>T
ENST00000381178.5:c.1070+17G>T	ENSP00000370571.1:n.1070+17G>T
ENST00000412076.1:c.136-67G>T
ENST00000416223.5:c.271+17G>T
ENST00000461172.1:n.142+17G>T
ENST00000479437.5:n.526+17G>T
NM_000360.3:c.977+17G>T	NP_000351.2:n.977+17G>T
NM_199292.2:c.1070+17G>T	NP_954986.2:n.1070+17G>T
NM_199293.2:c.1058+17G>T	NP_954987.2:n.1058+17G>T
XM_011520335.1:c.989+17G>T	XP_011518637.1:n.989+17G>T
XM_011520335.2:c.989+17G>T	XP_011518637.1:n.989+17G>T
NM_000360.4:c.977+17G>T MANE Select	NP_000351.2:n.977+17G>T
NM_199292.3:c.1070+17G>T	NP_954986.2:n.1070+17G>T
NM_199293.3:c.1058+17G>T	NP_954987.2:n.1058+17G>T