Canonical Allele Identifier: CA2699301996

Gene: THADA

Linked Data

• dbSNP Id: rs2105045875

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43494485C>G , CM000664.2:g.43494485C>G	GRCh38
NC_000002.11:g.43721624C>G , CM000664.1:g.43721624C>G	GRCh37
NC_000002.10:g.43575128C>G	NCBI36
NG_051580.1:g.106562G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405975.7:c.3744+4348G>C MANE Select	ENSP00000386088.2:n.3744+4348G>C
ENST00000398653.5:c.*2842+4348G>C	ENSP00000381647.1:n.*2842+4348G>C
ENST00000402796.5:c.2282+4348G>C	ENSP00000385003.1:n.2282+4348G>C
ENST00000405006.8:c.3744+4348G>C	ENSP00000385995.4:n.3744+4348G>C
ENST00000405975.6:c.3744+4348G>C	ENSP00000386088.2:n.3744+4348G>C
ENST00000407351.5:c.1685+4348G>C
ENST00000408045.7:c.*2839+4348G>C	ENSP00000384172.2:n.*2839+4348G>C
ENST00000436947.1:n.343+4348G>C
NM_001083953.1:c.3744+4348G>C	NP_001077422.1:n.3744+4348G>C
NM_022065.4:c.3744+4348G>C	NP_071348.3:n.3744+4348G>C
NR_073394.1:n.3876+4348G>C
XM_006712061.2:c.3744+4348G>C	XP_006712124.1:n.3744+4348G>C
XM_006712062.1:c.3741+4348G>C	XP_006712125.1:n.3741+4348G>C
XM_006712063.1:c.3624+4348G>C	XP_006712126.1:n.3624+4348G>C
XM_006712064.1:c.3744+4348G>C	XP_006712127.1:n.3744+4348G>C
XM_006712065.1:c.3744+4348G>C	XP_006712128.1:n.3744+4348G>C
XM_006712066.1:c.3381+4348G>C	XP_006712129.1:n.3381+4348G>C
XM_006712067.1:c.3378+4348G>C	XP_006712130.1:n.3378+4348G>C
XM_006712068.2:c.3744+4348G>C	XP_006712131.1:n.3744+4348G>C
XM_006712069.2:c.1293+4348G>C	XP_006712132.1:n.1293+4348G>C
XM_011533015.1:c.3744+4348G>C	XP_011531317.1:n.3744+4348G>C
XM_011533016.1:c.1056+4348G>C	XP_011531318.1:n.1056+4348G>C
NM_001345923.1:c.3741+4348G>C	NP_001332852.1:n.3741+4348G>C
NM_001345924.1:c.3621+4348G>C	NP_001332853.1:n.3621+4348G>C
NM_001345925.1:c.3744+4348G>C	NP_001332854.1:n.3744+4348G>C
NR_144316.1:n.3884+4348G>C
XM_006712064.2:c.3744+4348G>C	XP_006712127.1:n.3744+4348G>C
XM_006712068.3:c.3744+4348G>C	XP_006712131.1:n.3744+4348G>C
XM_006712069.3:c.1293+4348G>C	XP_006712132.1:n.1293+4348G>C
XM_011533015.3:c.3744+4348G>C	XP_011531317.1:n.3744+4348G>C
XM_017004675.1:c.1056+4348G>C	XP_016860164.1:n.1056+4348G>C
NM_001083953.2:c.3744+4348G>C	NP_001077422.1:n.3744+4348G>C
NM_001345923.2:c.3741+4348G>C	NP_001332852.1:n.3741+4348G>C
NM_001345924.2:c.3621+4348G>C	NP_001332853.1:n.3621+4348G>C
NM_001345925.2:c.3744+4348G>C	NP_001332854.1:n.3744+4348G>C
NM_022065.5:c.3744+4348G>C MANE Select	NP_071348.3:n.3744+4348G>C
NR_073394.2:n.3868+4348G>C
NR_144316.2:n.3876+4348G>C