Canonical Allele Identifier: CA461105729

Gene: CHD7

Linked Data

• MyVariant Identifiers: chr8:g.61777652A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60865093A>C , CM000670.2:g.60865093A>C	GRCh38
NC_000008.10:g.61777652A>C , CM000670.1:g.61777652A>C	GRCh37
NC_000008.9:g.61940206A>C	NCBI36
NG_007009.1:g.191314A>C , LRG_176:g.191314A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.1330A>C
ENST00000695852.1:n.261A>C
ENST00000695853.1:c.*1213A>C	ENSP00000512218.1:n.*1213A>C
ENST00000423902.7:c.8154A>C MANE Select	ENSP00000392028.1:p.Gly2718=
ENST00000423902.6:c.8154A>C	ENSP00000392028.1:p.Gly2718=
ENST00000524602.5:c.2007A>C	ENSP00000437061.1:p.Gly669=
ENST00000528280.1:n.200A>C
ENST00000532149.1:n.576A>C
ENST00000618450.1:n.4190A>C
NM_001316690.1:c.2007A>C	NP_001303619.1:p.Gly669=
NM_017780.3:c.8154A>C	NP_060250.2:p.Gly2718=
XM_011517553.1:c.8244A>C	XP_011515855.1:p.Gly2748=
XM_011517554.1:c.8244A>C	XP_011515856.1:p.Gly2748=
XM_011517555.1:c.8241A>C	XP_011515857.1:p.Gly2747=
XM_011517556.1:c.8022A>C	XP_011515858.1:p.Gly2674=
XM_011517557.1:c.6231A>C	XP_011515859.1:p.Gly2077=
XM_011517558.1:c.5781A>C	XP_011515860.1:p.Gly1927=
XM_011517559.1:c.4989A>C	XP_011515861.1:p.Gly1663=
XM_011517553.2:c.8244A>C	XP_011515855.1:p.Gly2748=
XM_011517554.3:c.8244A>C	XP_011515856.1:p.Gly2748=
XM_011517555.2:c.8241A>C	XP_011515857.1:p.Gly2747=
XM_017013612.1:c.8244A>C	XP_016869101.1:p.Gly2748=
XM_017013613.1:c.8151A>C	XP_016869102.1:p.Gly2717=
NM_017780.4:c.8154A>C MANE Select	NP_060250.2:p.Gly2718=