Canonical Allele Identifier: CA371299905

Gene: CHD7

Linked Data

• ClinVar Variation Id: 963065
• ClinVar RCV Id: RCV001237037
• dbSNP Id: rs1805714852
• MyVariant Identifiers: chr8:g.61769040A>T (hg19) ; chr8:g.60856481A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60856481A>T , CM000670.2:g.60856481A>T	GRCh38
NC_000008.10:g.61769040A>T , CM000670.1:g.61769040A>T	GRCh37
NC_000008.9:g.61931594A>T	NCBI36
NG_007009.1:g.182702A>T , LRG_176:g.182702A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.377A>T
ENST00000695853.1:c.*260A>T	ENSP00000512218.1:n.*260A>T
ENST00000423902.7:c.7201A>T MANE Select	ENSP00000392028.1:p.Arg2401Trp
ENST00000423902.6:c.7201A>T	ENSP00000392028.1:p.Arg2401Trp
ENST00000524602.5:c.1717-5748A>T	ENSP00000437061.1:n.1717-5748A>T
ENST00000529472.1:n.382A>T
NM_001316690.1:c.1717-5748A>T	NP_001303619.1:n.1717-5748A>T
NM_017780.3:c.7201A>T	NP_060250.2:p.Arg2401Trp
XM_011517553.1:c.7291A>T	XP_011515855.1:p.Arg2431Trp
XM_011517554.1:c.7291A>T	XP_011515856.1:p.Arg2431Trp
XM_011517555.1:c.7288A>T	XP_011515857.1:p.Arg2430Trp
XM_011517556.1:c.7291A>T	XP_011515858.1:p.Arg2431Trp
XM_011517557.1:c.5278A>T	XP_011515859.1:p.Arg1760Trp
XM_011517558.1:c.4828A>T	XP_011515860.1:p.Arg1610Trp
XM_011517559.1:c.4036A>T	XP_011515861.1:p.Arg1346Trp
XM_011517553.2:c.7291A>T	XP_011515855.1:p.Arg2431Trp
XM_011517554.3:c.7291A>T	XP_011515856.1:p.Arg2431Trp
XM_011517555.2:c.7288A>T	XP_011515857.1:p.Arg2430Trp
XM_017013612.1:c.7291A>T	XP_016869101.1:p.Arg2431Trp
XM_017013613.1:c.7198A>T	XP_016869102.1:p.Arg2400Trp
NM_017780.4:c.7201A>T MANE Select	NP_060250.2:p.Arg2401Trp