Canonical Allele Identifier: CA853921322

Gene: CHD7

Linked Data

• dbSNP Id: rs1194210551
• gnomAD v3: 8-60743423-TTCTTTC-T
• gnomAD v4: 8-60743423-TTCTTTC-T
• MyVariant Identifiers: chr8:g.61655983_61655988del (hg19) ; chr8:g.60743424_60743429del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60743431_60743436del , CM000670.2:g.60743431_60743436del	GRCh38
NC_000008.10:g.61655990_61655995del , CM000670.1:g.61655990_61655995del	GRCh37
NC_000008.9:g.61818544_61818549del	NCBI36
NG_007009.1:g.69652_69657del , LRG_176:g.69652_69657del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695848.1:n.2178+334_2178+339del
ENST00000695849.1:n.2178+334_2178+339del
ENST00000695853.1:c.1665+334_1665+339del	ENSP00000512218.1:n.1665+334_1665+339del
ENST00000700671.1:c.1665+334_1665+339del	ENSP00000515139.1:n.1665+334_1665+339del
ENST00000423902.7:c.1665+334_1665+339del MANE Select	ENSP00000392028.1:n.1665+334_1665+339del
ENST00000423902.6:c.1665+334_1665+339del	ENSP00000392028.1:n.1665+334_1665+339del
ENST00000524602.5:c.1665+334_1665+339del	ENSP00000437061.1:n.1665+334_1665+339del
ENST00000525508.1:c.1665+334_1665+339del	ENSP00000436027.1:n.1665+334_1665+339del
ENST00000527825.1:c.309+334_309+339del
ENST00000527900.1:c.66+334_66+339del	ENSP00000433336.1:n.66+334_66+339del
NM_001316690.1:c.1665+334_1665+339del	NP_001303619.1:n.1665+334_1665+339del
NM_017780.3:c.1665+334_1665+339del	NP_060250.2:n.1665+334_1665+339del
XM_011517553.1:c.1665+334_1665+339del	XP_011515855.1:n.1665+334_1665+339del
XM_011517554.1:c.1665+334_1665+339del	XP_011515856.1:n.1665+334_1665+339del
XM_011517555.1:c.1665+334_1665+339del	XP_011515857.1:n.1665+334_1665+339del
XM_011517556.1:c.1665+334_1665+339del	XP_011515858.1:n.1665+334_1665+339del
XM_011517560.1:c.1665+334_1665+339del	XP_011515862.1:n.1665+334_1665+339del
XM_011517553.2:c.1665+334_1665+339del	XP_011515855.1:n.1665+334_1665+339del
XM_011517554.3:c.1665+334_1665+339del	XP_011515856.1:n.1665+334_1665+339del
XM_011517555.2:c.1665+334_1665+339del	XP_011515857.1:n.1665+334_1665+339del
XM_011517560.2:c.1665+334_1665+339del	XP_011515862.1:n.1665+334_1665+339del
XM_017013612.1:c.1665+334_1665+339del	XP_016869101.1:n.1665+334_1665+339del
XM_017013613.1:c.1665+334_1665+339del	XP_016869102.1:n.1665+334_1665+339del
NM_017780.4:c.1665+334_1665+339del MANE Select	NP_060250.2:n.1665+334_1665+339del