Canonical Allele Identifier: CA461105746

Gene: CHD7

Linked Data

• MyVariant Identifiers: chr8:g.61777664A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60865105A>G , CM000670.2:g.60865105A>G	GRCh38
NC_000008.10:g.61777664A>G , CM000670.1:g.61777664A>G	GRCh37
NC_000008.9:g.61940218A>G	NCBI36
NG_007009.1:g.191326A>G , LRG_176:g.191326A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.1342A>G
ENST00000695852.1:n.273A>G
ENST00000695853.1:c.*1225A>G	ENSP00000512218.1:n.*1225A>G
ENST00000423902.7:c.8166A>G MANE Select	ENSP00000392028.1:p.Lys2722=
ENST00000423902.6:c.8166A>G	ENSP00000392028.1:p.Lys2722=
ENST00000524602.5:c.2019A>G	ENSP00000437061.1:p.Lys673=
ENST00000528280.1:n.212A>G
ENST00000532149.1:n.588A>G
ENST00000618450.1:n.4202A>G
NM_001316690.1:c.2019A>G	NP_001303619.1:p.Lys673=
NM_017780.3:c.8166A>G	NP_060250.2:p.Lys2722=
XM_011517553.1:c.8256A>G	XP_011515855.1:p.Lys2752=
XM_011517554.1:c.8256A>G	XP_011515856.1:p.Lys2752=
XM_011517555.1:c.8253A>G	XP_011515857.1:p.Lys2751=
XM_011517556.1:c.8034A>G	XP_011515858.1:p.Lys2678=
XM_011517557.1:c.6243A>G	XP_011515859.1:p.Lys2081=
XM_011517558.1:c.5793A>G	XP_011515860.1:p.Lys1931=
XM_011517559.1:c.5001A>G	XP_011515861.1:p.Lys1667=
XM_011517553.2:c.8256A>G	XP_011515855.1:p.Lys2752=
XM_011517554.3:c.8256A>G	XP_011515856.1:p.Lys2752=
XM_011517555.2:c.8253A>G	XP_011515857.1:p.Lys2751=
XM_017013612.1:c.8256A>G	XP_016869101.1:p.Lys2752=
XM_017013613.1:c.8163A>G	XP_016869102.1:p.Lys2721=
NM_017780.4:c.8166A>G MANE Select	NP_060250.2:p.Lys2722=