Canonical Allele Identifier: CA371310173

Gene: CHD7

Linked Data

• MyVariant Identifiers: chr8:g.61778022A>C (hg19) ; chr8:g.60865463A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60865463A>C , CM000670.2:g.60865463A>C	GRCh38
NC_000008.10:g.61778022A>C , CM000670.1:g.61778022A>C	GRCh37
NC_000008.9:g.61940576A>C	NCBI36
NG_007009.1:g.191684A>C , LRG_176:g.191684A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.1700A>C
ENST00000695852.1:n.631A>C
ENST00000695853.1:c.*1583A>C	ENSP00000512218.1:n.*1583A>C
ENST00000423902.7:c.8524A>C MANE Select	ENSP00000392028.1:p.Lys2842Gln
ENST00000423902.6:c.8524A>C	ENSP00000392028.1:p.Lys2842Gln
ENST00000524602.5:c.2377A>C	ENSP00000437061.1:p.Lys793Gln
NM_001316690.1:c.2377A>C	NP_001303619.1:p.Lys793Gln
NM_017780.3:c.8524A>C	NP_060250.2:p.Lys2842Gln
XM_011517553.1:c.8614A>C	XP_011515855.1:p.Lys2872Gln
XM_011517554.1:c.8614A>C	XP_011515856.1:p.Lys2872Gln
XM_011517555.1:c.8611A>C	XP_011515857.1:p.Lys2871Gln
XM_011517556.1:c.8392A>C	XP_011515858.1:p.Lys2798Gln
XM_011517557.1:c.6601A>C	XP_011515859.1:p.Lys2201Gln
XM_011517558.1:c.6151A>C	XP_011515860.1:p.Lys2051Gln
XM_011517559.1:c.5359A>C	XP_011515861.1:p.Lys1787Gln
XM_011517553.2:c.8614A>C	XP_011515855.1:p.Lys2872Gln
XM_011517554.3:c.8614A>C	XP_011515856.1:p.Lys2872Gln
XM_011517555.2:c.8611A>C	XP_011515857.1:p.Lys2871Gln
XM_017013612.1:c.8614A>C	XP_016869101.1:p.Lys2872Gln
XM_017013613.1:c.8521A>C	XP_016869102.1:p.Lys2841Gln
NM_017780.4:c.8524A>C MANE Select	NP_060250.2:p.Lys2842Gln