Canonical Allele Identifier: CA371309988

Gene: CHD7

Linked Data

• ClinVar Variation Id: 488373
• ClinVar RCV Id: RCV000578162 ; RCV000578888
• dbSNP Id: rs1554597716
• MyVariant Identifiers: chr8:g.61735210C>T (hg19) ; chr8:g.60822651C>T (hg38)
• PubMed: PMID:29300383

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60822651C>T , CM000670.2:g.60822651C>T	GRCh38
NC_000008.10:g.61735210C>T , CM000670.1:g.61735210C>T	GRCh37
NC_000008.9:g.61897764C>T	NCBI36
NG_007009.1:g.148872C>T , LRG_176:g.148872C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000695853.1:c.3106C>T	ENSP00000512218.1:p.Arg1036Ter
ENST00000423902.7:c.3106C>T MANE Select	ENSP00000392028.1:p.Arg1036Ter
ENST00000423902.6:c.3106C>T	ENSP00000392028.1:p.Arg1036Ter
ENST00000524602.5:c.1717-39578C>T	ENSP00000437061.1:n.1717-39578C>T
ENST00000525508.1:c.3106C>T	ENSP00000436027.1:p.Arg1036Ter
NM_001316690.1:c.1717-39578C>T	NP_001303619.1:n.1717-39578C>T
NM_017780.3:c.3106C>T	NP_060250.2:p.Arg1036Ter
XM_011517553.1:c.3106C>T	XP_011515855.1:p.Arg1036Ter
XM_011517554.1:c.3106C>T	XP_011515856.1:p.Arg1036Ter
XM_011517555.1:c.3106C>T	XP_011515857.1:p.Arg1036Ter
XM_011517556.1:c.3106C>T	XP_011515858.1:p.Arg1036Ter
XM_011517557.1:c.1093C>T	XP_011515859.1:p.Arg365Ter
XM_011517558.1:c.643C>T	XP_011515860.1:p.Arg215Ter
XM_011517560.1:c.3106C>T	XP_011515862.1:p.Arg1036Ter
XM_011517553.2:c.3106C>T	XP_011515855.1:p.Arg1036Ter
XM_011517554.3:c.3106C>T	XP_011515856.1:p.Arg1036Ter
XM_011517555.2:c.3106C>T	XP_011515857.1:p.Arg1036Ter
XM_011517560.2:c.3106C>T	XP_011515862.1:p.Arg1036Ter
XM_017013612.1:c.3106C>T	XP_016869101.1:p.Arg1036Ter
XM_017013613.1:c.3106C>T	XP_016869102.1:p.Arg1036Ter
NM_017780.4:c.3106C>T MANE Select	NP_060250.2:p.Arg1036Ter