Canonical Allele Identifier: CA460846401

Gene: CHD7

Linked Data

• MyVariant Identifiers: chr8:g.61773486T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60860927T>G , CM000670.2:g.60860927T>G	GRCh38
NC_000008.10:g.61773486T>G , CM000670.1:g.61773486T>G	GRCh37
NC_000008.9:g.61936040T>G	NCBI36
NG_007009.1:g.187148T>G , LRG_176:g.187148T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000695850.1:n.808T>G
ENST00000695851.1:n.12T>G
ENST00000695853.1:c.*691T>G	ENSP00000512218.1:n.*691T>G
ENST00000423902.7:c.7632T>G MANE Select	ENSP00000392028.1:p.Ala2544=
ENST00000423902.6:c.7632T>G	ENSP00000392028.1:p.Ala2544=
ENST00000524602.5:c.1717-1302T>G	ENSP00000437061.1:n.1717-1302T>G
ENST00000531695.1:n.56T>G
ENST00000618450.1:n.24T>G
NM_001316690.1:c.1717-1302T>G	NP_001303619.1:n.1717-1302T>G
NM_017780.3:c.7632T>G	NP_060250.2:p.Ala2544=
XM_011517553.1:c.7722T>G	XP_011515855.1:p.Ala2574=
XM_011517554.1:c.7722T>G	XP_011515856.1:p.Ala2574=
XM_011517555.1:c.7719T>G	XP_011515857.1:p.Ala2573=
XM_011517556.1:c.7699-1269T>G	XP_011515858.1:n.7699-1269T>G
XM_011517557.1:c.5709T>G	XP_011515859.1:p.Ala1903=
XM_011517558.1:c.5259T>G	XP_011515860.1:p.Ala1753=
XM_011517559.1:c.4467T>G	XP_011515861.1:p.Ala1489=
XM_011517553.2:c.7722T>G	XP_011515855.1:p.Ala2574=
XM_011517554.3:c.7722T>G	XP_011515856.1:p.Ala2574=
XM_011517555.2:c.7719T>G	XP_011515857.1:p.Ala2573=
XM_017013612.1:c.7722T>G	XP_016869101.1:p.Ala2574=
XM_017013613.1:c.7629T>G	XP_016869102.1:p.Ala2543=
NM_017780.4:c.7632T>G MANE Select	NP_060250.2:p.Ala2544=