Canonical Allele Identifier: CA397944729

Gene: CHD3

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7905098A>G , CM000679.2:g.7905098A>G	GRCh38
NC_000017.10:g.7808416A>G , CM000679.1:g.7808416A>G	GRCh37
NC_000017.9:g.7749141A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001005273.3:c.4073-2A>G MANE Select	NP_001005273.1:n.4073-2A>G
ENST00000330494.12:c.4073-2A>G MANE Select	ENSP00000332628.7:n.4073-2A>G
NM_001005271.2:c.4250-2A>G	NP_001005271.2:n.4250-2A>G
NM_001005271.3:c.4250-2A>G	NP_001005271.2:n.4250-2A>G
NM_001005273.2:c.4073-2A>G	NP_001005273.1:n.4073-2A>G
NM_005852.3:c.4073-2A>G	NP_005843.2:n.4073-2A>G
NM_005852.4:c.4073-2A>G	NP_005843.2:n.4073-2A>G
ENST00000330494.11:c.4073-2A>G	ENSP00000332628.7:n.4073-2A>G
ENST00000358181.8:c.4073-2A>G	ENSP00000350907.4:n.4073-2A>G
ENST00000380358.8:c.4250-2A>G	ENSP00000369716.4:n.4250-2A>G
ENST00000380358.9:c.4250-2A>G	ENSP00000369716.4:n.4250-2A>G
ENST00000466233.1:n.547-2A>G
ENST00000470531.5:c.636-2A>G	ENSP00000467547.1:n.636-2A>G
ENST00000473376.1:n.386-2A>G
ENST00000672838.1:c.4007-2A>G	ENSP00000500734.1:n.4007-2A>G
ENST00000682063.1:n.1247-2A>G
ENST00000700753.1:c.4250-2A>G	ENSP00000515165.1:n.4250-2A>G
XM_005256427.3:c.4250-2A>G	XP_005256484.1:n.4250-2A>G
XM_005256427.4:c.4250-2A>G	XP_005256484.1:n.4250-2A>G
XM_005256428.3:c.4250-2A>G	XP_005256485.1:n.4250-2A>G
XM_005256428.4:c.4250-2A>G	XP_005256485.1:n.4250-2A>G
XM_005256429.3:c.4250-2A>G	XP_005256486.1:n.4250-2A>G
XM_005256429.4:c.4250-2A>G	XP_005256486.1:n.4250-2A>G
XM_006721423.2:c.4250-2A>G	XP_006721486.1:n.4250-2A>G
XM_006721423.3:c.4250-2A>G	XP_006721486.1:n.4250-2A>G
XM_006721424.2:c.4238-2A>G	XP_006721487.1:n.4238-2A>G
XM_006721424.3:c.4238-2A>G	XP_006721487.1:n.4238-2A>G
XM_006721425.2:c.3980-2A>G	XP_006721488.2:n.3980-2A>G
XM_006721427.2:c.4013-2A>G	XP_006721490.1:n.4013-2A>G
XM_006721428.2:c.4250-2A>G	XP_006721491.1:n.4250-2A>G
XM_006721428.3:c.4250-2A>G	XP_006721491.1:n.4250-2A>G
XM_006721430.2:c.4238-2A>G	XP_006721493.1:n.4238-2A>G
XM_011523628.1:c.4040-2A>G	XP_011521930.1:n.4040-2A>G
XM_011523629.1:c.4040-2A>G	XP_011521931.1:n.4040-2A>G
XM_011523630.1:c.3980-2A>G	XP_011521932.1:n.3980-2A>G
XM_017024061.1:c.4232-2A>G	XP_016879550.1:n.4232-2A>G
XM_017024062.1:c.4220-2A>G	XP_016879551.1:n.4220-2A>G
XM_017024063.1:c.4073-2A>G	XP_016879552.1:n.4073-2A>G
XM_017024064.1:c.4238-2A>G	XP_016879553.1:n.4238-2A>G
XM_017024065.1:c.4046-2A>G	XP_016879554.1:n.4046-2A>G
XM_017024066.1:c.4013-2A>G	XP_016879555.1:n.4013-2A>G
XM_017024067.2:c.4040-2A>G	XP_016879556.1:n.4040-2A>G
XM_017024068.1:c.4013-2A>G	XP_016879557.1:n.4013-2A>G
XM_017024069.1:c.3569-2A>G	XP_016879558.1:n.3569-2A>G
XM_017024070.1:c.4220-2A>G	XP_016879559.1:n.4220-2A>G