Canonical Allele Identifier: CA1788134966

Gene: CHD7

Linked Data

• dbSNP Id: rs1805345020

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60849189_60849190insAAAGACAACATTTATAAGAAA , CM000670.2:g.60849189_60849190insAAAGACAACATTTATAAGAAA	GRCh38
NC_000008.10:g.61761748_61761749insAAAGACAACATTTATAAGAAA , CM000670.1:g.61761748_61761749insAAAGACAACATTTATAAGAAA	GRCh37
NC_000008.9:g.61924302_61924303insAAAGACAACATTTATAAGAAA	NCBI36
NG_007009.1:g.175410_175411insAAAGACAACATTTATAAGAAA , LRG_176:g.175410_175411insAAAGACAACATTTATAAGAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695853.1:c.5404+35_5404+36insAAAGACAACATTTATAAGAAA	ENSP00000512218.1:n.5404+35_5404+36insAAAGACAACATTTATAAGAAA
ENST00000423902.7:c.5404+35_5404+36insAAAGACAACATTTATAAGAAA MANE Select	ENSP00000392028.1:n.5404+35_5404+36insAAAGACAACATTTATAAGAAA
ENST00000423902.6:c.5404+35_5404+36insAAAGACAACATTTATAAGAAA	ENSP00000392028.1:n.5404+35_5404+36insAAAGACAACATTTATAAGAAA
ENST00000524602.5:c.1717-13040_1717-13039insAAAGACAACATTTATAAGAAA	ENSP00000437061.1:n.1717-13040_1717-13039insAAAGACAACATTTATAA...
NM_001316690.1:c.1717-13040_1717-13039insAAAGACAACATTTATAAGAAA	NP_001303619.1:n.1717-13040_1717-13039insAAAGACAACATTTATAAGAA...
NM_017780.3:c.5404+35_5404+36insAAAGACAACATTTATAAGAAA	NP_060250.2:n.5404+35_5404+36insAAAGACAACATTTATAAGAAA
XM_011517553.1:c.5494+35_5494+36insAAAGACAACATTTATAAGAAA	XP_011515855.1:n.5494+35_5494+36insAAAGACAACATTTATAAGAAA
XM_011517554.1:c.5494+35_5494+36insAAAGACAACATTTATAAGAAA	XP_011515856.1:n.5494+35_5494+36insAAAGACAACATTTATAAGAAA
XM_011517555.1:c.5494+35_5494+36insAAAGACAACATTTATAAGAAA	XP_011515857.1:n.5494+35_5494+36insAAAGACAACATTTATAAGAAA
XM_011517556.1:c.5494+35_5494+36insAAAGACAACATTTATAAGAAA	XP_011515858.1:n.5494+35_5494+36insAAAGACAACATTTATAAGAAA
XM_011517557.1:c.3481+35_3481+36insAAAGACAACATTTATAAGAAA	XP_011515859.1:n.3481+35_3481+36insAAAGACAACATTTATAAGAAA
XM_011517558.1:c.3031+35_3031+36insAAAGACAACATTTATAAGAAA	XP_011515860.1:n.3031+35_3031+36insAAAGACAACATTTATAAGAAA
XM_011517559.1:c.2239+35_2239+36insAAAGACAACATTTATAAGAAA	XP_011515861.1:n.2239+35_2239+36insAAAGACAACATTTATAAGAAA
XM_011517553.2:c.5494+35_5494+36insAAAGACAACATTTATAAGAAA	XP_011515855.1:n.5494+35_5494+36insAAAGACAACATTTATAAGAAA
XM_011517554.3:c.5494+35_5494+36insAAAGACAACATTTATAAGAAA	XP_011515856.1:n.5494+35_5494+36insAAAGACAACATTTATAAGAAA
XM_011517555.2:c.5494+35_5494+36insAAAGACAACATTTATAAGAAA	XP_011515857.1:n.5494+35_5494+36insAAAGACAACATTTATAAGAAA
XM_017013612.1:c.5494+35_5494+36insAAAGACAACATTTATAAGAAA	XP_016869101.1:n.5494+35_5494+36insAAAGACAACATTTATAAGAAA
XM_017013613.1:c.5404+35_5404+36insAAAGACAACATTTATAAGAAA	XP_016869102.1:n.5404+35_5404+36insAAAGACAACATTTATAAGAAA
NM_017780.4:c.5404+35_5404+36insAAAGACAACATTTATAAGAAA MANE Select	NP_060250.2:n.5404+35_5404+36insAAAGACAACATTTATAAGAAA