Canonical Allele Identifier: CA2695209400

Gene: CHD7

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60852644dup , CM000670.2:g.60852644dup	GRCh38
NC_000008.10:g.61765203dup , CM000670.1:g.61765203dup	GRCh37
NC_000008.9:g.61927757dup	NCBI36
NG_007009.1:g.178865dup , LRG_176:g.178865dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695853.1:c.6041dup	ENSP00000512218.1:p.Tyr2014Ter
ENST00000423902.7:c.6041dup MANE Select	ENSP00000392028.1:p.Tyr2014Ter
ENST00000423902.6:c.6041dup	ENSP00000392028.1:p.Tyr2014Ter
ENST00000524602.5:c.1717-9585dup	ENSP00000437061.1:n.1717-9585dup
NM_001316690.1:c.1717-9585dup	NP_001303619.1:n.1717-9585dup
NM_017780.3:c.6041dup	NP_060250.2:p.Tyr2014Ter
XM_011517553.1:c.6131dup	XP_011515855.1:p.Tyr2044Ter
XM_011517554.1:c.6131dup	XP_011515856.1:p.Tyr2044Ter
XM_011517555.1:c.6131dup	XP_011515857.1:p.Tyr2044Ter
XM_011517556.1:c.6131dup	XP_011515858.1:p.Tyr2044Ter
XM_011517557.1:c.4118dup	XP_011515859.1:p.Tyr1373Ter
XM_011517558.1:c.3668dup	XP_011515860.1:p.Tyr1223Ter
XM_011517559.1:c.2876dup	XP_011515861.1:p.Tyr959Ter
XM_011517553.2:c.6131dup	XP_011515855.1:p.Tyr2044Ter
XM_011517554.3:c.6131dup	XP_011515856.1:p.Tyr2044Ter
XM_011517555.2:c.6131dup	XP_011515857.1:p.Tyr2044Ter
XM_017013612.1:c.6131dup	XP_016869101.1:p.Tyr2044Ter
XM_017013613.1:c.6041dup	XP_016869102.1:p.Tyr2014Ter
NM_017780.4:c.6041dup MANE Select	NP_060250.2:p.Tyr2014Ter