Canonical Allele Identifier: CA371308466

Gene: CHD7

Linked Data

• dbSNP Id: rs762731699
• MyVariant Identifiers: chr8:g.61777831G>C (hg19) ; chr8:g.60865272G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60865272G>C , CM000670.2:g.60865272G>C	GRCh38
NC_000008.10:g.61777831G>C , CM000670.1:g.61777831G>C	GRCh37
NC_000008.9:g.61940385G>C	NCBI36
NG_007009.1:g.191493G>C , LRG_176:g.191493G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.1509G>C
ENST00000695852.1:n.440G>C
ENST00000695853.1:c.*1392G>C	ENSP00000512218.1:n.*1392G>C
ENST00000423902.7:c.8333G>C MANE Select	ENSP00000392028.1:p.Gly2778Ala
ENST00000423902.6:c.8333G>C	ENSP00000392028.1:p.Gly2778Ala
ENST00000524602.5:c.2186G>C	ENSP00000437061.1:p.Gly729Ala
ENST00000528280.1:n.379G>C
NM_001316690.1:c.2186G>C	NP_001303619.1:p.Gly729Ala
NM_017780.3:c.8333G>C	NP_060250.2:p.Gly2778Ala
XM_011517553.1:c.8423G>C	XP_011515855.1:p.Gly2808Ala
XM_011517554.1:c.8423G>C	XP_011515856.1:p.Gly2808Ala
XM_011517555.1:c.8420G>C	XP_011515857.1:p.Gly2807Ala
XM_011517556.1:c.8201G>C	XP_011515858.1:p.Gly2734Ala
XM_011517557.1:c.6410G>C	XP_011515859.1:p.Gly2137Ala
XM_011517558.1:c.5960G>C	XP_011515860.1:p.Gly1987Ala
XM_011517559.1:c.5168G>C	XP_011515861.1:p.Gly1723Ala
XM_011517553.2:c.8423G>C	XP_011515855.1:p.Gly2808Ala
XM_011517554.3:c.8423G>C	XP_011515856.1:p.Gly2808Ala
XM_011517555.2:c.8420G>C	XP_011515857.1:p.Gly2807Ala
XM_017013612.1:c.8423G>C	XP_016869101.1:p.Gly2808Ala
XM_017013613.1:c.8330G>C	XP_016869102.1:p.Gly2777Ala
NM_017780.4:c.8333G>C MANE Select	NP_060250.2:p.Gly2778Ala