Canonical Allele Identifier: CA371320465

Gene: CHD7

Linked Data

• ClinVar Variation Id: 2836523
• ClinVar RCV Id: RCV003604650
• MyVariant Identifiers: chr8:g.61757882G>C (hg19) ; chr8:g.60845323G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60845323G>C , CM000670.2:g.60845323G>C	GRCh38
NC_000008.10:g.61757882G>C , CM000670.1:g.61757882G>C	GRCh37
NC_000008.9:g.61920436G>C	NCBI36
NG_007009.1:g.171544G>C , LRG_176:g.171544G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695853.1:c.5124G>C	ENSP00000512218.1:p.Gln1708His
ENST00000423902.7:c.5124G>C MANE Select	ENSP00000392028.1:p.Gln1708His
ENST00000423902.6:c.5124G>C	ENSP00000392028.1:p.Gln1708His
ENST00000524602.5:c.1717-16906G>C	ENSP00000437061.1:n.1717-16906G>C
NM_001316690.1:c.1717-16906G>C	NP_001303619.1:n.1717-16906G>C
NM_017780.3:c.5124G>C	NP_060250.2:p.Gln1708His
XM_011517553.1:c.5124G>C	XP_011515855.1:p.Gln1708His
XM_011517554.1:c.5124G>C	XP_011515856.1:p.Gln1708His
XM_011517555.1:c.5124G>C	XP_011515857.1:p.Gln1708His
XM_011517556.1:c.5124G>C	XP_011515858.1:p.Gln1708His
XM_011517557.1:c.3111G>C	XP_011515859.1:p.Gln1037His
XM_011517558.1:c.2661G>C	XP_011515860.1:p.Gln887His
XM_011517559.1:c.1869G>C	XP_011515861.1:p.Gln623His
XM_011517553.2:c.5124G>C	XP_011515855.1:p.Gln1708His
XM_011517554.3:c.5124G>C	XP_011515856.1:p.Gln1708His
XM_011517555.2:c.5124G>C	XP_011515857.1:p.Gln1708His
XM_017013612.1:c.5124G>C	XP_016869101.1:p.Gln1708His
XM_017013613.1:c.5124G>C	XP_016869102.1:p.Gln1708His
NM_017780.4:c.5124G>C MANE Select	NP_060250.2:p.Gln1708His