Canonical Allele Identifier: CA371310359

Gene: CHD7

Linked Data

• MyVariant Identifiers: chr8:g.61778038G>T (hg19) ; chr8:g.60865479G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60865479G>T , CM000670.2:g.60865479G>T	GRCh38
NC_000008.10:g.61778038G>T , CM000670.1:g.61778038G>T	GRCh37
NC_000008.9:g.61940592G>T	NCBI36
NG_007009.1:g.191700G>T , LRG_176:g.191700G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.1716G>T
ENST00000695852.1:n.647G>T
ENST00000695853.1:c.*1599G>T	ENSP00000512218.1:n.*1599G>T
ENST00000423902.7:c.8540G>T MANE Select	ENSP00000392028.1:p.Gly2847Val
ENST00000423902.6:c.8540G>T	ENSP00000392028.1:p.Gly2847Val
ENST00000524602.5:c.2393G>T	ENSP00000437061.1:p.Gly798Val
NM_001316690.1:c.2393G>T	NP_001303619.1:p.Gly798Val
NM_017780.3:c.8540G>T	NP_060250.2:p.Gly2847Val
XM_011517553.1:c.8630G>T	XP_011515855.1:p.Gly2877Val
XM_011517554.1:c.8630G>T	XP_011515856.1:p.Gly2877Val
XM_011517555.1:c.8627G>T	XP_011515857.1:p.Gly2876Val
XM_011517556.1:c.8408G>T	XP_011515858.1:p.Gly2803Val
XM_011517557.1:c.6617G>T	XP_011515859.1:p.Gly2206Val
XM_011517558.1:c.6167G>T	XP_011515860.1:p.Gly2056Val
XM_011517559.1:c.5375G>T	XP_011515861.1:p.Gly1792Val
XM_011517553.2:c.8630G>T	XP_011515855.1:p.Gly2877Val
XM_011517554.3:c.8630G>T	XP_011515856.1:p.Gly2877Val
XM_011517555.2:c.8627G>T	XP_011515857.1:p.Gly2876Val
XM_017013612.1:c.8630G>T	XP_016869101.1:p.Gly2877Val
XM_017013613.1:c.8537G>T	XP_016869102.1:p.Gly2846Val
NM_017780.4:c.8540G>T MANE Select	NP_060250.2:p.Gly2847Val