Canonical Allele Identifier: CA2780535155
Gene: CHD7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.60848496_60848497dup , CM000670.2:g.60848496_60848497dup GRCh38
NC_000008.10:g.61761055_61761056dup , CM000670.1:g.61761055_61761056dup GRCh37
NC_000008.9:g.61923609_61923610dup NCBI36
NG_007009.1:g.174717_174718dup , LRG_176:g.174717_174718dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000695853.1:c.5211-19_5211-18dup ENSP00000512218.1:n.5211-19_5211-18dup
ENST00000423902.7:c.5211-19_5211-18dup MANE Select ENSP00000392028.1:n.5211-19_5211-18dup
ENST00000423902.6:c.5211-19_5211-18dup ENSP00000392028.1:n.5211-19_5211-18dup
ENST00000524602.5:c.1717-13733_1717-13732dup ENSP00000437061.1:n.1717-13733_1717-13732dup
NM_001316690.1:c.1717-13733_1717-13732dup NP_001303619.1:n.1717-13733_1717-13732dup
NM_017780.3:c.5211-19_5211-18dup NP_060250.2:n.5211-19_5211-18dup
XM_011517553.1:c.5301-19_5301-18dup XP_011515855.1:n.5301-19_5301-18dup
XM_011517554.1:c.5301-19_5301-18dup XP_011515856.1:n.5301-19_5301-18dup
XM_011517555.1:c.5301-19_5301-18dup XP_011515857.1:n.5301-19_5301-18dup
XM_011517556.1:c.5301-19_5301-18dup XP_011515858.1:n.5301-19_5301-18dup
XM_011517557.1:c.3288-19_3288-18dup XP_011515859.1:n.3288-19_3288-18dup
XM_011517558.1:c.2838-19_2838-18dup XP_011515860.1:n.2838-19_2838-18dup
XM_011517559.1:c.2046-19_2046-18dup XP_011515861.1:n.2046-19_2046-18dup
XM_011517553.2:c.5301-19_5301-18dup XP_011515855.1:n.5301-19_5301-18dup
XM_011517554.3:c.5301-19_5301-18dup XP_011515856.1:n.5301-19_5301-18dup
XM_011517555.2:c.5301-19_5301-18dup XP_011515857.1:n.5301-19_5301-18dup
XM_017013612.1:c.5301-19_5301-18dup XP_016869101.1:n.5301-19_5301-18dup
XM_017013613.1:c.5211-19_5211-18dup XP_016869102.1:n.5211-19_5211-18dup
NM_017780.4:c.5211-19_5211-18dup MANE Select NP_060250.2:n.5211-19_5211-18dup