Canonical Allele Identifier: CA371307630

Gene: CHD7

Linked Data

• MyVariant Identifiers: chr8:g.61777687C>G (hg19) ; chr8:g.60865128C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60865128C>G , CM000670.2:g.60865128C>G	GRCh38
NC_000008.10:g.61777687C>G , CM000670.1:g.61777687C>G	GRCh37
NC_000008.9:g.61940241C>G	NCBI36
NG_007009.1:g.191349C>G , LRG_176:g.191349C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.1365C>G
ENST00000695852.1:n.296C>G
ENST00000695853.1:c.*1248C>G	ENSP00000512218.1:n.*1248C>G
ENST00000423902.7:c.8189C>G MANE Select	ENSP00000392028.1:p.Ala2730Gly
ENST00000423902.6:c.8189C>G	ENSP00000392028.1:p.Ala2730Gly
ENST00000524602.5:c.2042C>G	ENSP00000437061.1:p.Ala681Gly
ENST00000528280.1:n.235C>G
ENST00000532149.1:n.611C>G
NM_001316690.1:c.2042C>G	NP_001303619.1:p.Ala681Gly
NM_017780.3:c.8189C>G	NP_060250.2:p.Ala2730Gly
XM_011517553.1:c.8279C>G	XP_011515855.1:p.Ala2760Gly
XM_011517554.1:c.8279C>G	XP_011515856.1:p.Ala2760Gly
XM_011517555.1:c.8276C>G	XP_011515857.1:p.Ala2759Gly
XM_011517556.1:c.8057C>G	XP_011515858.1:p.Ala2686Gly
XM_011517557.1:c.6266C>G	XP_011515859.1:p.Ala2089Gly
XM_011517558.1:c.5816C>G	XP_011515860.1:p.Ala1939Gly
XM_011517559.1:c.5024C>G	XP_011515861.1:p.Ala1675Gly
XM_011517553.2:c.8279C>G	XP_011515855.1:p.Ala2760Gly
XM_011517554.3:c.8279C>G	XP_011515856.1:p.Ala2760Gly
XM_011517555.2:c.8276C>G	XP_011515857.1:p.Ala2759Gly
XM_017013612.1:c.8279C>G	XP_016869101.1:p.Ala2760Gly
XM_017013613.1:c.8186C>G	XP_016869102.1:p.Ala2729Gly
NM_017780.4:c.8189C>G MANE Select	NP_060250.2:p.Ala2730Gly