Canonical Allele Identifier: CA1788129222

Gene: CHD7

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60865127G= , CM000670.2:g.60865127G=	GRCh38
NC_000008.10:g.61777686G= , CM000670.1:g.61777686G=	GRCh37
NC_000008.9:g.61940240G=	NCBI36
NG_007009.1:g.191348G= , LRG_176:g.191348G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.1364G=
ENST00000695852.1:n.295G=
ENST00000695853.1:c.*1247G=	ENSP00000512218.1:n.*1247G=
ENST00000423902.7:c.8188G= MANE Select	ENSP00000392028.1:p.Ala2730=
ENST00000423902.6:c.8188G=	ENSP00000392028.1:p.Ala2730=
ENST00000524602.5:c.2041G=	ENSP00000437061.1:p.Ala681=
ENST00000528280.1:n.234G=
ENST00000532149.1:n.610G=
NM_001316690.1:c.2041G=	NP_001303619.1:p.Ala681=
NM_017780.3:c.8188G=	NP_060250.2:p.Ala2730=
XM_011517553.1:c.8278G=	XP_011515855.1:p.Ala2760=
XM_011517554.1:c.8278G=	XP_011515856.1:p.Ala2760=
XM_011517555.1:c.8275G=	XP_011515857.1:p.Ala2759=
XM_011517556.1:c.8056G=	XP_011515858.1:p.Ala2686=
XM_011517557.1:c.6265G=	XP_011515859.1:p.Ala2089=
XM_011517558.1:c.5815G=	XP_011515860.1:p.Ala1939=
XM_011517559.1:c.5023G=	XP_011515861.1:p.Ala1675=
XM_011517553.2:c.8278G=	XP_011515855.1:p.Ala2760=
XM_011517554.3:c.8278G=	XP_011515856.1:p.Ala2760=
XM_011517555.2:c.8275G=	XP_011515857.1:p.Ala2759=
XM_017013612.1:c.8278G=	XP_016869101.1:p.Ala2760=
XM_017013613.1:c.8185G=	XP_016869102.1:p.Ala2729=
NM_017780.4:c.8188G= MANE Select	NP_060250.2:p.Ala2730=