Canonical Allele Identifier: CA2695209582

Gene: CHD7

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60743042_60743043insA , CM000670.2:g.60743042_60743043insA	GRCh38
NC_000008.10:g.61655601_61655602insA , CM000670.1:g.61655601_61655602insA	GRCh37
NC_000008.9:g.61818155_61818156insA	NCBI36
NG_007009.1:g.69263_69264insA , LRG_176:g.69263_69264insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695848.1:n.2123_2124insA
ENST00000695849.1:n.2123_2124insA
ENST00000695853.1:c.1610_1611insA	ENSP00000512218.1:p.Trp537Ter
ENST00000700671.1:c.1610_1611insA	ENSP00000515139.1:p.Trp537Ter
ENST00000423902.7:c.1610_1611insA MANE Select	ENSP00000392028.1:p.Trp537Ter
ENST00000423902.6:c.1610_1611insA	ENSP00000392028.1:p.Trp537Ter
ENST00000524602.5:c.1610_1611insA	ENSP00000437061.1:p.Trp537Ter
ENST00000525508.1:c.1610_1611insA	ENSP00000436027.1:p.Trp537Ter
ENST00000527825.1:c.254_255insA
ENST00000527900.1:c.11_12insA	ENSP00000433336.1:p.Trp4Ter
NM_001316690.1:c.1610_1611insA	NP_001303619.1:p.Trp537Ter
NM_017780.3:c.1610_1611insA	NP_060250.2:p.Trp537Ter
XM_011517553.1:c.1610_1611insA	XP_011515855.1:p.Trp537Ter
XM_011517554.1:c.1610_1611insA	XP_011515856.1:p.Trp537Ter
XM_011517555.1:c.1610_1611insA	XP_011515857.1:p.Trp537Ter
XM_011517556.1:c.1610_1611insA	XP_011515858.1:p.Trp537Ter
XM_011517560.1:c.1610_1611insA	XP_011515862.1:p.Trp537Ter
XM_011517553.2:c.1610_1611insA	XP_011515855.1:p.Trp537Ter
XM_011517554.3:c.1610_1611insA	XP_011515856.1:p.Trp537Ter
XM_011517555.2:c.1610_1611insA	XP_011515857.1:p.Trp537Ter
XM_011517560.2:c.1610_1611insA	XP_011515862.1:p.Trp537Ter
XM_017013612.1:c.1610_1611insA	XP_016869101.1:p.Trp537Ter
XM_017013613.1:c.1610_1611insA	XP_016869102.1:p.Trp537Ter
NM_017780.4:c.1610_1611insA MANE Select	NP_060250.2:p.Trp537Ter