Canonical Allele Identifier: CA2749695176

Gene: THADA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43494442_43494443insCT , CM000664.2:g.43494442_43494443insCT	GRCh38
NC_000002.11:g.43721581_43721582insCT , CM000664.1:g.43721581_43721582insCT	GRCh37
NC_000002.10:g.43575085_43575086insCT	NCBI36
NG_051580.1:g.106604_106605insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405975.7:c.3744+4390_3744+4391insAG MANE Select	ENSP00000386088.2:n.3744+4390_3744+4391insAG
ENST00000398653.5:c.*2842+4390_*2842+4391insAG	ENSP00000381647.1:n.*2842+4390_*2842+4391insAG
ENST00000402796.5:c.2282+4390_2282+4391insAG	ENSP00000385003.1:n.2282+4390_2282+4391insAG
ENST00000405006.8:c.3744+4390_3744+4391insAG	ENSP00000385995.4:n.3744+4390_3744+4391insAG
ENST00000405975.6:c.3744+4390_3744+4391insAG	ENSP00000386088.2:n.3744+4390_3744+4391insAG
ENST00000407351.5:c.1685+4390_1685+4391insAG
ENST00000408045.7:c.*2839+4390_*2839+4391insAG	ENSP00000384172.2:n.*2839+4390_*2839+4391insAG
ENST00000436947.1:n.343+4390_343+4391insAG
NM_001083953.1:c.3744+4390_3744+4391insAG	NP_001077422.1:n.3744+4390_3744+4391insAG
NM_022065.4:c.3744+4390_3744+4391insAG	NP_071348.3:n.3744+4390_3744+4391insAG
NR_073394.1:n.3876+4390_3876+4391insAG
XM_006712061.2:c.3744+4390_3744+4391insAG	XP_006712124.1:n.3744+4390_3744+4391insAG
XM_006712062.1:c.3741+4390_3741+4391insAG	XP_006712125.1:n.3741+4390_3741+4391insAG
XM_006712063.1:c.3624+4390_3624+4391insAG	XP_006712126.1:n.3624+4390_3624+4391insAG
XM_006712064.1:c.3744+4390_3744+4391insAG	XP_006712127.1:n.3744+4390_3744+4391insAG
XM_006712065.1:c.3744+4390_3744+4391insAG	XP_006712128.1:n.3744+4390_3744+4391insAG
XM_006712066.1:c.3381+4390_3381+4391insAG	XP_006712129.1:n.3381+4390_3381+4391insAG
XM_006712067.1:c.3378+4390_3378+4391insAG	XP_006712130.1:n.3378+4390_3378+4391insAG
XM_006712068.2:c.3744+4390_3744+4391insAG	XP_006712131.1:n.3744+4390_3744+4391insAG
XM_006712069.2:c.1293+4390_1293+4391insAG	XP_006712132.1:n.1293+4390_1293+4391insAG
XM_011533015.1:c.3744+4390_3744+4391insAG	XP_011531317.1:n.3744+4390_3744+4391insAG
XM_011533016.1:c.1056+4390_1056+4391insAG	XP_011531318.1:n.1056+4390_1056+4391insAG
NM_001345923.1:c.3741+4390_3741+4391insAG	NP_001332852.1:n.3741+4390_3741+4391insAG
NM_001345924.1:c.3621+4390_3621+4391insAG	NP_001332853.1:n.3621+4390_3621+4391insAG
NM_001345925.1:c.3744+4390_3744+4391insAG	NP_001332854.1:n.3744+4390_3744+4391insAG
NR_144316.1:n.3884+4390_3884+4391insAG
XM_006712064.2:c.3744+4390_3744+4391insAG	XP_006712127.1:n.3744+4390_3744+4391insAG
XM_006712068.3:c.3744+4390_3744+4391insAG	XP_006712131.1:n.3744+4390_3744+4391insAG
XM_006712069.3:c.1293+4390_1293+4391insAG	XP_006712132.1:n.1293+4390_1293+4391insAG
XM_011533015.3:c.3744+4390_3744+4391insAG	XP_011531317.1:n.3744+4390_3744+4391insAG
XM_017004675.1:c.1056+4390_1056+4391insAG	XP_016860164.1:n.1056+4390_1056+4391insAG
NM_001083953.2:c.3744+4390_3744+4391insAG	NP_001077422.1:n.3744+4390_3744+4391insAG
NM_001345923.2:c.3741+4390_3741+4391insAG	NP_001332852.1:n.3741+4390_3741+4391insAG
NM_001345924.2:c.3621+4390_3621+4391insAG	NP_001332853.1:n.3621+4390_3621+4391insAG
NM_001345925.2:c.3744+4390_3744+4391insAG	NP_001332854.1:n.3744+4390_3744+4391insAG
NM_022065.5:c.3744+4390_3744+4391insAG MANE Select	NP_071348.3:n.3744+4390_3744+4391insAG
NR_073394.2:n.3868+4390_3868+4391insAG
NR_144316.2:n.3876+4390_3876+4391insAG