Canonical Allele Identifier: CA1788103513

Gene: CHD7

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60853060C= , CM000670.2:g.60853060C=	GRCh38
NC_000008.10:g.61765619C= , CM000670.1:g.61765619C=	GRCh37
NC_000008.9:g.61928173C=	NCBI36
NG_007009.1:g.179281C= , LRG_176:g.179281C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000695853.1:c.6335C=	ENSP00000512218.1:p.Thr2112=
ENST00000423902.7:c.6335C= MANE Select	ENSP00000392028.1:p.Thr2112=
ENST00000423902.6:c.6335C=	ENSP00000392028.1:p.Thr2112=
ENST00000524602.5:c.1717-9169C=	ENSP00000437061.1:n.1717-9169C=
NM_001316690.1:c.1717-9169C=	NP_001303619.1:n.1717-9169C=
NM_017780.3:c.6335C=	NP_060250.2:p.Thr2112=
XM_011517553.1:c.6425C=	XP_011515855.1:p.Thr2142=
XM_011517554.1:c.6425C=	XP_011515856.1:p.Thr2142=
XM_011517555.1:c.6425C=	XP_011515857.1:p.Thr2142=
XM_011517556.1:c.6425C=	XP_011515858.1:p.Thr2142=
XM_011517557.1:c.4412C=	XP_011515859.1:p.Thr1471=
XM_011517558.1:c.3962C=	XP_011515860.1:p.Thr1321=
XM_011517559.1:c.3170C=	XP_011515861.1:p.Thr1057=
XM_011517553.2:c.6425C=	XP_011515855.1:p.Thr2142=
XM_011517554.3:c.6425C=	XP_011515856.1:p.Thr2142=
XM_011517555.2:c.6425C=	XP_011515857.1:p.Thr2142=
XM_017013612.1:c.6425C=	XP_016869101.1:p.Thr2142=
XM_017013613.1:c.6335C=	XP_016869102.1:p.Thr2112=
NM_017780.4:c.6335C= MANE Select	NP_060250.2:p.Thr2112=