Canonical Allele Identifier: CA371304598

Gene: CHD7

Linked Data

• MyVariant Identifiers: chr8:g.61773598G>T (hg19) ; chr8:g.60861039G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60861039G>T , CM000670.2:g.60861039G>T	GRCh38
NC_000008.10:g.61773598G>T , CM000670.1:g.61773598G>T	GRCh37
NC_000008.9:g.61936152G>T	NCBI36
NG_007009.1:g.187260G>T , LRG_176:g.187260G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.920G>T
ENST00000695851.1:n.124G>T
ENST00000695853.1:c.*803G>T	ENSP00000512218.1:n.*803G>T
ENST00000423902.7:c.7744G>T MANE Select	ENSP00000392028.1:p.Gly2582Trp
ENST00000423902.6:c.7744G>T	ENSP00000392028.1:p.Gly2582Trp
ENST00000524602.5:c.1717-1190G>T	ENSP00000437061.1:n.1717-1190G>T
ENST00000531695.1:n.168G>T
ENST00000618450.1:n.136G>T
NM_001316690.1:c.1717-1190G>T	NP_001303619.1:n.1717-1190G>T
NM_017780.3:c.7744G>T	NP_060250.2:p.Gly2582Trp
XM_011517553.1:c.7834G>T	XP_011515855.1:p.Gly2612Trp
XM_011517554.1:c.7834G>T	XP_011515856.1:p.Gly2612Trp
XM_011517555.1:c.7831G>T	XP_011515857.1:p.Gly2611Trp
XM_011517556.1:c.7699-1157G>T	XP_011515858.1:n.7699-1157G>T
XM_011517557.1:c.5821G>T	XP_011515859.1:p.Gly1941Trp
XM_011517558.1:c.5371G>T	XP_011515860.1:p.Gly1791Trp
XM_011517559.1:c.4579G>T	XP_011515861.1:p.Gly1527Trp
XM_011517553.2:c.7834G>T	XP_011515855.1:p.Gly2612Trp
XM_011517554.3:c.7834G>T	XP_011515856.1:p.Gly2612Trp
XM_011517555.2:c.7831G>T	XP_011515857.1:p.Gly2611Trp
XM_017013612.1:c.7834G>T	XP_016869101.1:p.Gly2612Trp
XM_017013613.1:c.7741G>T	XP_016869102.1:p.Gly2581Trp
NM_017780.4:c.7744G>T MANE Select	NP_060250.2:p.Gly2582Trp