Canonical Allele Identifier: CA461105720

Gene: CHD7

Linked Data

• MyVariant Identifiers: chr8:g.61777643C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60865084C>T , CM000670.2:g.60865084C>T	GRCh38
NC_000008.10:g.61777643C>T , CM000670.1:g.61777643C>T	GRCh37
NC_000008.9:g.61940197C>T	NCBI36
NG_007009.1:g.191305C>T , LRG_176:g.191305C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.1321C>T
ENST00000695852.1:n.252C>T
ENST00000695853.1:c.*1204C>T	ENSP00000512218.1:n.*1204C>T
ENST00000423902.7:c.8145C>T MANE Select	ENSP00000392028.1:p.Ser2715=
ENST00000423902.6:c.8145C>T	ENSP00000392028.1:p.Ser2715=
ENST00000524602.5:c.1998C>T	ENSP00000437061.1:p.Ser666=
ENST00000528280.1:n.191C>T
ENST00000532149.1:n.567C>T
ENST00000618450.1:n.4181C>T
NM_001316690.1:c.1998C>T	NP_001303619.1:p.Ser666=
NM_017780.3:c.8145C>T	NP_060250.2:p.Ser2715=
XM_011517553.1:c.8235C>T	XP_011515855.1:p.Ser2745=
XM_011517554.1:c.8235C>T	XP_011515856.1:p.Ser2745=
XM_011517555.1:c.8232C>T	XP_011515857.1:p.Ser2744=
XM_011517556.1:c.8013C>T	XP_011515858.1:p.Ser2671=
XM_011517557.1:c.6222C>T	XP_011515859.1:p.Ser2074=
XM_011517558.1:c.5772C>T	XP_011515860.1:p.Ser1924=
XM_011517559.1:c.4980C>T	XP_011515861.1:p.Ser1660=
XM_011517553.2:c.8235C>T	XP_011515855.1:p.Ser2745=
XM_011517554.3:c.8235C>T	XP_011515856.1:p.Ser2745=
XM_011517555.2:c.8232C>T	XP_011515857.1:p.Ser2744=
XM_017013612.1:c.8235C>T	XP_016869101.1:p.Ser2745=
XM_017013613.1:c.8142C>T	XP_016869102.1:p.Ser2714=
NM_017780.4:c.8145C>T MANE Select	NP_060250.2:p.Ser2715=