Canonical Allele Identifier: CA371304552

Gene: CHD7

Linked Data

• MyVariant Identifiers: chr8:g.61773577G>C (hg19) ; chr8:g.60861018G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60861018G>C , CM000670.2:g.60861018G>C	GRCh38
NC_000008.10:g.61773577G>C , CM000670.1:g.61773577G>C	GRCh37
NC_000008.9:g.61936131G>C	NCBI36
NG_007009.1:g.187239G>C , LRG_176:g.187239G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.899G>C
ENST00000695851.1:n.103G>C
ENST00000695853.1:c.*782G>C	ENSP00000512218.1:n.*782G>C
ENST00000423902.7:c.7723G>C MANE Select	ENSP00000392028.1:p.Glu2575Gln
ENST00000423902.6:c.7723G>C	ENSP00000392028.1:p.Glu2575Gln
ENST00000524602.5:c.1717-1211G>C	ENSP00000437061.1:n.1717-1211G>C
ENST00000531695.1:n.147G>C
ENST00000618450.1:n.115G>C
NM_001316690.1:c.1717-1211G>C	NP_001303619.1:n.1717-1211G>C
NM_017780.3:c.7723G>C	NP_060250.2:p.Glu2575Gln
XM_011517553.1:c.7813G>C	XP_011515855.1:p.Glu2605Gln
XM_011517554.1:c.7813G>C	XP_011515856.1:p.Glu2605Gln
XM_011517555.1:c.7810G>C	XP_011515857.1:p.Glu2604Gln
XM_011517556.1:c.7699-1178G>C	XP_011515858.1:n.7699-1178G>C
XM_011517557.1:c.5800G>C	XP_011515859.1:p.Glu1934Gln
XM_011517558.1:c.5350G>C	XP_011515860.1:p.Glu1784Gln
XM_011517559.1:c.4558G>C	XP_011515861.1:p.Glu1520Gln
XM_011517553.2:c.7813G>C	XP_011515855.1:p.Glu2605Gln
XM_011517554.3:c.7813G>C	XP_011515856.1:p.Glu2605Gln
XM_011517555.2:c.7810G>C	XP_011515857.1:p.Glu2604Gln
XM_017013612.1:c.7813G>C	XP_016869101.1:p.Glu2605Gln
XM_017013613.1:c.7720G>C	XP_016869102.1:p.Glu2574Gln
NM_017780.4:c.7723G>C MANE Select	NP_060250.2:p.Glu2575Gln