Canonical Allele Identifier: CA4760083

Gene: CHD7

Linked Data

• dbSNP Id: rs776775999
• ExAC: 8:61749485 A / C
• gnomAD v4: 8-60836926-A-C
• MyVariant Identifiers: chr8:g.61749485A>C (hg19) ; chr8:g.60836926A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60836926A>C , CM000670.2:g.60836926A>C	GRCh38
NC_000008.10:g.61749485A>C , CM000670.1:g.61749485A>C	GRCh37
NC_000008.9:g.61912039A>C	NCBI36
NG_007009.1:g.163147A>C , LRG_176:g.163147A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000695853.1:c.4099A>C	ENSP00000512218.1:p.Arg1367=
ENST00000423902.7:c.4099A>C MANE Select	ENSP00000392028.1:p.Arg1367=
ENST00000423902.6:c.4099A>C	ENSP00000392028.1:p.Arg1367=
ENST00000524602.5:c.1717-25303A>C	ENSP00000437061.1:n.1717-25303A>C
NM_001316690.1:c.1717-25303A>C	NP_001303619.1:n.1717-25303A>C
NM_017780.3:c.4099A>C	NP_060250.2:p.Arg1367=
XM_011517553.1:c.4099A>C	XP_011515855.1:p.Arg1367=
XM_011517554.1:c.4099A>C	XP_011515856.1:p.Arg1367=
XM_011517555.1:c.4099A>C	XP_011515857.1:p.Arg1367=
XM_011517556.1:c.4099A>C	XP_011515858.1:p.Arg1367=
XM_011517557.1:c.2086A>C	XP_011515859.1:p.Arg696=
XM_011517558.1:c.1636A>C	XP_011515860.1:p.Arg546=
XM_011517559.1:c.844A>C	XP_011515861.1:p.Arg282=
XM_011517560.1:c.4099A>C	XP_011515862.1:p.Arg1367=
XM_011517553.2:c.4099A>C	XP_011515855.1:p.Arg1367=
XM_011517554.3:c.4099A>C	XP_011515856.1:p.Arg1367=
XM_011517555.2:c.4099A>C	XP_011515857.1:p.Arg1367=
XM_011517560.2:c.4099A>C	XP_011515862.1:p.Arg1367=
XM_017013612.1:c.4099A>C	XP_016869101.1:p.Arg1367=
XM_017013613.1:c.4099A>C	XP_016869102.1:p.Arg1367=
NM_017780.4:c.4099A>C MANE Select	NP_060250.2:p.Arg1367=