Canonical Allele Identifier: CA371325981

Gene: CHD7

Linked Data

• ClinVar Variation Id: 2506851
• ClinVar RCV Id: RCV003237220
• dbSNP Id: rs1405897510
• gnomAD v2: 8-61765910-C-T
• gnomAD v3: 8-60853351-C-T
• gnomAD v4: 8-60853351-C-T
• MyVariant Identifiers: chr8:g.61765910C>T (hg19) ; chr8:g.60853351C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60853351C>T , CM000670.2:g.60853351C>T	GRCh38
NC_000008.10:g.61765910C>T , CM000670.1:g.61765910C>T	GRCh37
NC_000008.9:g.61928464C>T	NCBI36
NG_007009.1:g.179572C>T , LRG_176:g.179572C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695853.1:c.6626C>T	ENSP00000512218.1:p.Ala2209Val
ENST00000423902.7:c.6626C>T MANE Select	ENSP00000392028.1:p.Ala2209Val
ENST00000423902.6:c.6626C>T	ENSP00000392028.1:p.Ala2209Val
ENST00000524602.5:c.1717-8878C>T	ENSP00000437061.1:n.1717-8878C>T
NM_001316690.1:c.1717-8878C>T	NP_001303619.1:n.1717-8878C>T
NM_017780.3:c.6626C>T	NP_060250.2:p.Ala2209Val
XM_011517553.1:c.6716C>T	XP_011515855.1:p.Ala2239Val
XM_011517554.1:c.6716C>T	XP_011515856.1:p.Ala2239Val
XM_011517555.1:c.6716C>T	XP_011515857.1:p.Ala2239Val
XM_011517556.1:c.6716C>T	XP_011515858.1:p.Ala2239Val
XM_011517557.1:c.4703C>T	XP_011515859.1:p.Ala1568Val
XM_011517558.1:c.4253C>T	XP_011515860.1:p.Ala1418Val
XM_011517559.1:c.3461C>T	XP_011515861.1:p.Ala1154Val
XM_011517553.2:c.6716C>T	XP_011515855.1:p.Ala2239Val
XM_011517554.3:c.6716C>T	XP_011515856.1:p.Ala2239Val
XM_011517555.2:c.6716C>T	XP_011515857.1:p.Ala2239Val
XM_017013612.1:c.6716C>T	XP_016869101.1:p.Ala2239Val
XM_017013613.1:c.6626C>T	XP_016869102.1:p.Ala2209Val
NM_017780.4:c.6626C>T MANE Select	NP_060250.2:p.Ala2209Val