Canonical Allele Identifier: CA4760594

Gene: CHD7

Linked Data

• ClinVar Variation Id: 695939
• ClinVar RCV Id: RCV000861986 ; RCV001195447 ; RCV001655612 ; RCV002507464
• dbSNP Id: rs777858802
• ExAC: 8:61765752 C / T
• gnomAD v2: 8-61765752-C-T
• gnomAD v3: 8-60853193-C-T
• gnomAD v4: 8-60853193-C-T
• MyVariant Identifiers: chr8:g.61765752C>T (hg19) ; chr8:g.60853193C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60853193C>T , CM000670.2:g.60853193C>T	GRCh38
NC_000008.10:g.61765752C>T , CM000670.1:g.61765752C>T	GRCh37
NC_000008.9:g.61928306C>T	NCBI36
NG_007009.1:g.179414C>T , LRG_176:g.179414C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695853.1:c.6468C>T	ENSP00000512218.1:p.Val2156=
ENST00000423902.7:c.6468C>T MANE Select	ENSP00000392028.1:p.Val2156=
ENST00000423902.6:c.6468C>T	ENSP00000392028.1:p.Val2156=
ENST00000524602.5:c.1717-9036C>T	ENSP00000437061.1:n.1717-9036C>T
NM_001316690.1:c.1717-9036C>T	NP_001303619.1:n.1717-9036C>T
NM_017780.3:c.6468C>T	NP_060250.2:p.Val2156=
XM_011517553.1:c.6558C>T	XP_011515855.1:p.Val2186=
XM_011517554.1:c.6558C>T	XP_011515856.1:p.Val2186=
XM_011517555.1:c.6558C>T	XP_011515857.1:p.Val2186=
XM_011517556.1:c.6558C>T	XP_011515858.1:p.Val2186=
XM_011517557.1:c.4545C>T	XP_011515859.1:p.Val1515=
XM_011517558.1:c.4095C>T	XP_011515860.1:p.Val1365=
XM_011517559.1:c.3303C>T	XP_011515861.1:p.Val1101=
XM_011517553.2:c.6558C>T	XP_011515855.1:p.Val2186=
XM_011517554.3:c.6558C>T	XP_011515856.1:p.Val2186=
XM_011517555.2:c.6558C>T	XP_011515857.1:p.Val2186=
XM_017013612.1:c.6558C>T	XP_016869101.1:p.Val2186=
XM_017013613.1:c.6468C>T	XP_016869102.1:p.Val2156=
NM_017780.4:c.6468C>T MANE Select	NP_060250.2:p.Val2156=