Canonical Allele Identifier: CA371309925

Gene: CHD7

Linked Data

• MyVariant Identifiers: chr8:g.61777994T>G (hg19) ; chr8:g.60865435T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60865435T>G , CM000670.2:g.60865435T>G	GRCh38
NC_000008.10:g.61777994T>G , CM000670.1:g.61777994T>G	GRCh37
NC_000008.9:g.61940548T>G	NCBI36
NG_007009.1:g.191656T>G , LRG_176:g.191656T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.1672T>G
ENST00000695852.1:n.603T>G
ENST00000695853.1:c.*1555T>G	ENSP00000512218.1:n.*1555T>G
ENST00000423902.7:c.8496T>G MANE Select	ENSP00000392028.1:p.Ser2832Arg
ENST00000423902.6:c.8496T>G	ENSP00000392028.1:p.Ser2832Arg
ENST00000524602.5:c.2349T>G	ENSP00000437061.1:p.Ser783Arg
ENST00000528280.1:n.542T>G
NM_001316690.1:c.2349T>G	NP_001303619.1:p.Ser783Arg
NM_017780.3:c.8496T>G	NP_060250.2:p.Ser2832Arg
XM_011517553.1:c.8586T>G	XP_011515855.1:p.Ser2862Arg
XM_011517554.1:c.8586T>G	XP_011515856.1:p.Ser2862Arg
XM_011517555.1:c.8583T>G	XP_011515857.1:p.Ser2861Arg
XM_011517556.1:c.8364T>G	XP_011515858.1:p.Ser2788Arg
XM_011517557.1:c.6573T>G	XP_011515859.1:p.Ser2191Arg
XM_011517558.1:c.6123T>G	XP_011515860.1:p.Ser2041Arg
XM_011517559.1:c.5331T>G	XP_011515861.1:p.Ser1777Arg
XM_011517553.2:c.8586T>G	XP_011515855.1:p.Ser2862Arg
XM_011517554.3:c.8586T>G	XP_011515856.1:p.Ser2862Arg
XM_011517555.2:c.8583T>G	XP_011515857.1:p.Ser2861Arg
XM_017013612.1:c.8586T>G	XP_016869101.1:p.Ser2862Arg
XM_017013613.1:c.8493T>G	XP_016869102.1:p.Ser2831Arg
NM_017780.4:c.8496T>G MANE Select	NP_060250.2:p.Ser2832Arg