Canonical Allele Identifier: CA241726

Gene: CHD7

Linked Data

• ClinVar Variation Id: 195335
• ClinVar RCV Id: RCV000175897 ; RCV003497838 ; RCV004020086
• dbSNP Id: rs748842029
• ExAC: 8:61655635 G / A
• gnomAD v2: 8-61655635-G-A
• gnomAD v3: 8-60743076-G-A
• gnomAD v4: 8-60743076-G-A
• MyVariant Identifiers: chr8:g.61655635G>A (hg19) ; chr8:g.60743076G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60743076G>A , CM000670.2:g.60743076G>A	GRCh38
NC_000008.10:g.61655635G>A , CM000670.1:g.61655635G>A	GRCh37
NC_000008.9:g.61818189G>A	NCBI36
NG_007009.1:g.69297G>A , LRG_176:g.69297G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695848.1:n.2157G>A
ENST00000695849.1:n.2157G>A
ENST00000695853.1:c.1644G>A	ENSP00000512218.1:p.Pro548=
ENST00000700671.1:c.1644G>A	ENSP00000515139.1:p.Pro548=
ENST00000423902.7:c.1644G>A MANE Select	ENSP00000392028.1:p.Pro548=
ENST00000423902.6:c.1644G>A	ENSP00000392028.1:p.Pro548=
ENST00000524602.5:c.1644G>A	ENSP00000437061.1:p.Pro548=
ENST00000525508.1:c.1644G>A	ENSP00000436027.1:p.Pro548=
ENST00000527825.1:c.288G>A
ENST00000527900.1:c.45G>A	ENSP00000433336.1:p.Pro15=
NM_001316690.1:c.1644G>A	NP_001303619.1:p.Pro548=
NM_017780.3:c.1644G>A	NP_060250.2:p.Pro548=
XM_011517553.1:c.1644G>A	XP_011515855.1:p.Pro548=
XM_011517554.1:c.1644G>A	XP_011515856.1:p.Pro548=
XM_011517555.1:c.1644G>A	XP_011515857.1:p.Pro548=
XM_011517556.1:c.1644G>A	XP_011515858.1:p.Pro548=
XM_011517560.1:c.1644G>A	XP_011515862.1:p.Pro548=
XM_011517553.2:c.1644G>A	XP_011515855.1:p.Pro548=
XM_011517554.3:c.1644G>A	XP_011515856.1:p.Pro548=
XM_011517555.2:c.1644G>A	XP_011515857.1:p.Pro548=
XM_011517560.2:c.1644G>A	XP_011515862.1:p.Pro548=
XM_017013612.1:c.1644G>A	XP_016869101.1:p.Pro548=
XM_017013613.1:c.1644G>A	XP_016869102.1:p.Pro548=
NM_017780.4:c.1644G>A MANE Select	NP_060250.2:p.Pro548=