Canonical Allele Identifier: CA371304646

Gene: CHD7

Linked Data

• MyVariant Identifiers: chr8:g.61773619A>C (hg19) ; chr8:g.60861060A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60861060A>C , CM000670.2:g.60861060A>C	GRCh38
NC_000008.10:g.61773619A>C , CM000670.1:g.61773619A>C	GRCh37
NC_000008.9:g.61936173A>C	NCBI36
NG_007009.1:g.187281A>C , LRG_176:g.187281A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.941A>C
ENST00000695851.1:n.145A>C
ENST00000695853.1:c.*824A>C	ENSP00000512218.1:n.*824A>C
ENST00000423902.7:c.7765A>C MANE Select	ENSP00000392028.1:p.Lys2589Gln
ENST00000423902.6:c.7765A>C	ENSP00000392028.1:p.Lys2589Gln
ENST00000524602.5:c.1717-1169A>C	ENSP00000437061.1:n.1717-1169A>C
ENST00000531695.1:n.189A>C
ENST00000618450.1:n.157A>C
NM_001316690.1:c.1717-1169A>C	NP_001303619.1:n.1717-1169A>C
NM_017780.3:c.7765A>C	NP_060250.2:p.Lys2589Gln
XM_011517553.1:c.7855A>C	XP_011515855.1:p.Lys2619Gln
XM_011517554.1:c.7855A>C	XP_011515856.1:p.Lys2619Gln
XM_011517555.1:c.7852A>C	XP_011515857.1:p.Lys2618Gln
XM_011517556.1:c.7699-1136A>C	XP_011515858.1:n.7699-1136A>C
XM_011517557.1:c.5842A>C	XP_011515859.1:p.Lys1948Gln
XM_011517558.1:c.5392A>C	XP_011515860.1:p.Lys1798Gln
XM_011517559.1:c.4600A>C	XP_011515861.1:p.Lys1534Gln
XM_011517553.2:c.7855A>C	XP_011515855.1:p.Lys2619Gln
XM_011517554.3:c.7855A>C	XP_011515856.1:p.Lys2619Gln
XM_011517555.2:c.7852A>C	XP_011515857.1:p.Lys2618Gln
XM_017013612.1:c.7855A>C	XP_016869101.1:p.Lys2619Gln
XM_017013613.1:c.7762A>C	XP_016869102.1:p.Lys2588Gln
NM_017780.4:c.7765A>C MANE Select	NP_060250.2:p.Lys2589Gln