Canonical Allele Identifier: CA371304601

Gene: CHD7

Linked Data

• MyVariant Identifiers: chr8:g.61773599G>T (hg19) ; chr8:g.60861040G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60861040G>T , CM000670.2:g.60861040G>T	GRCh38
NC_000008.10:g.61773599G>T , CM000670.1:g.61773599G>T	GRCh37
NC_000008.9:g.61936153G>T	NCBI36
NG_007009.1:g.187261G>T , LRG_176:g.187261G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.921G>T
ENST00000695851.1:n.125G>T
ENST00000695853.1:c.*804G>T	ENSP00000512218.1:n.*804G>T
ENST00000423902.7:c.7745G>T MANE Select	ENSP00000392028.1:p.Gly2582Val
ENST00000423902.6:c.7745G>T	ENSP00000392028.1:p.Gly2582Val
ENST00000524602.5:c.1717-1189G>T	ENSP00000437061.1:n.1717-1189G>T
ENST00000531695.1:n.169G>T
ENST00000618450.1:n.137G>T
NM_001316690.1:c.1717-1189G>T	NP_001303619.1:n.1717-1189G>T
NM_017780.3:c.7745G>T	NP_060250.2:p.Gly2582Val
XM_011517553.1:c.7835G>T	XP_011515855.1:p.Gly2612Val
XM_011517554.1:c.7835G>T	XP_011515856.1:p.Gly2612Val
XM_011517555.1:c.7832G>T	XP_011515857.1:p.Gly2611Val
XM_011517556.1:c.7699-1156G>T	XP_011515858.1:n.7699-1156G>T
XM_011517557.1:c.5822G>T	XP_011515859.1:p.Gly1941Val
XM_011517558.1:c.5372G>T	XP_011515860.1:p.Gly1791Val
XM_011517559.1:c.4580G>T	XP_011515861.1:p.Gly1527Val
XM_011517553.2:c.7835G>T	XP_011515855.1:p.Gly2612Val
XM_011517554.3:c.7835G>T	XP_011515856.1:p.Gly2612Val
XM_011517555.2:c.7832G>T	XP_011515857.1:p.Gly2611Val
XM_017013612.1:c.7835G>T	XP_016869101.1:p.Gly2612Val
XM_017013613.1:c.7742G>T	XP_016869102.1:p.Gly2581Val
NM_017780.4:c.7745G>T MANE Select	NP_060250.2:p.Gly2582Val