Canonical Allele Identifier: CA371304145

Gene: CHD7

Linked Data

• MyVariant Identifiers: chr8:g.61773472G>T (hg19) ; chr8:g.60860913G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60860913G>T , CM000670.2:g.60860913G>T	GRCh38
NC_000008.10:g.61773472G>T , CM000670.1:g.61773472G>T	GRCh37
NC_000008.9:g.61936026G>T	NCBI36
NG_007009.1:g.187134G>T , LRG_176:g.187134G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.794G>T
ENST00000695853.1:c.*677G>T	ENSP00000512218.1:n.*677G>T
ENST00000423902.7:c.7618G>T MANE Select	ENSP00000392028.1:p.Glu2540Ter
ENST00000423902.6:c.7618G>T	ENSP00000392028.1:p.Glu2540Ter
ENST00000524602.5:c.1717-1316G>T	ENSP00000437061.1:n.1717-1316G>T
ENST00000531695.1:n.42G>T
ENST00000618450.1:n.10G>T
NM_001316690.1:c.1717-1316G>T	NP_001303619.1:n.1717-1316G>T
NM_017780.3:c.7618G>T	NP_060250.2:p.Glu2540Ter
XM_011517553.1:c.7708G>T	XP_011515855.1:p.Glu2570Ter
XM_011517554.1:c.7708G>T	XP_011515856.1:p.Glu2570Ter
XM_011517555.1:c.7705G>T	XP_011515857.1:p.Glu2569Ter
XM_011517556.1:c.7699-1283G>T	XP_011515858.1:n.7699-1283G>T
XM_011517557.1:c.5695G>T	XP_011515859.1:p.Glu1899Ter
XM_011517558.1:c.5245G>T	XP_011515860.1:p.Glu1749Ter
XM_011517559.1:c.4453G>T	XP_011515861.1:p.Glu1485Ter
XM_011517553.2:c.7708G>T	XP_011515855.1:p.Glu2570Ter
XM_011517554.3:c.7708G>T	XP_011515856.1:p.Glu2570Ter
XM_011517555.2:c.7705G>T	XP_011515857.1:p.Glu2569Ter
XM_017013612.1:c.7708G>T	XP_016869101.1:p.Glu2570Ter
XM_017013613.1:c.7615G>T	XP_016869102.1:p.Glu2539Ter
NM_017780.4:c.7618G>T MANE Select	NP_060250.2:p.Glu2540Ter