Canonical Allele Identifier: CA371307359

Gene: CHD7

Linked Data

• MyVariant Identifiers: chr8:g.61777639C>G (hg19) ; chr8:g.60865080C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60865080C>G , CM000670.2:g.60865080C>G	GRCh38
NC_000008.10:g.61777639C>G , CM000670.1:g.61777639C>G	GRCh37
NC_000008.9:g.61940193C>G	NCBI36
NG_007009.1:g.191301C>G , LRG_176:g.191301C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.1317C>G
ENST00000695852.1:n.248C>G
ENST00000695853.1:c.*1200C>G	ENSP00000512218.1:n.*1200C>G
ENST00000423902.7:c.8141C>G MANE Select	ENSP00000392028.1:p.Ala2714Gly
ENST00000423902.6:c.8141C>G	ENSP00000392028.1:p.Ala2714Gly
ENST00000524602.5:c.1994C>G	ENSP00000437061.1:p.Ala665Gly
ENST00000528280.1:n.187C>G
ENST00000532149.1:n.563C>G
ENST00000618450.1:n.4177C>G
NM_001316690.1:c.1994C>G	NP_001303619.1:p.Ala665Gly
NM_017780.3:c.8141C>G	NP_060250.2:p.Ala2714Gly
XM_011517553.1:c.8231C>G	XP_011515855.1:p.Ala2744Gly
XM_011517554.1:c.8231C>G	XP_011515856.1:p.Ala2744Gly
XM_011517555.1:c.8228C>G	XP_011515857.1:p.Ala2743Gly
XM_011517556.1:c.8009C>G	XP_011515858.1:p.Ala2670Gly
XM_011517557.1:c.6218C>G	XP_011515859.1:p.Ala2073Gly
XM_011517558.1:c.5768C>G	XP_011515860.1:p.Ala1923Gly
XM_011517559.1:c.4976C>G	XP_011515861.1:p.Ala1659Gly
XM_011517553.2:c.8231C>G	XP_011515855.1:p.Ala2744Gly
XM_011517554.3:c.8231C>G	XP_011515856.1:p.Ala2744Gly
XM_011517555.2:c.8228C>G	XP_011515857.1:p.Ala2743Gly
XM_017013612.1:c.8231C>G	XP_016869101.1:p.Ala2744Gly
XM_017013613.1:c.8138C>G	XP_016869102.1:p.Ala2713Gly
NM_017780.4:c.8141C>G MANE Select	NP_060250.2:p.Ala2714Gly