Canonical Allele Identifier: CA371307495
Gene: CHD7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.60865109G>T , CM000670.2:g.60865109G>T GRCh38
NC_000008.10:g.61777668G>T , CM000670.1:g.61777668G>T GRCh37
NC_000008.9:g.61940222G>T NCBI36
NG_007009.1:g.191330G>T , LRG_176:g.191330G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000695850.1:n.1346G>T
ENST00000695852.1:n.277G>T
ENST00000695853.1:c.*1229G>T ENSP00000512218.1:n.*1229G>T
ENST00000423902.7:c.8170G>T MANE Select ENSP00000392028.1:p.Glu2724Ter
ENST00000423902.6:c.8170G>T ENSP00000392028.1:p.Glu2724Ter
ENST00000524602.5:c.2023G>T ENSP00000437061.1:p.Glu675Ter
ENST00000528280.1:n.216G>T
ENST00000532149.1:n.592G>T
ENST00000618450.1:n.4206G>T
NM_001316690.1:c.2023G>T NP_001303619.1:p.Glu675Ter
NM_017780.3:c.8170G>T NP_060250.2:p.Glu2724Ter
XM_011517553.1:c.8260G>T XP_011515855.1:p.Glu2754Ter
XM_011517554.1:c.8260G>T XP_011515856.1:p.Glu2754Ter
XM_011517555.1:c.8257G>T XP_011515857.1:p.Glu2753Ter
XM_011517556.1:c.8038G>T XP_011515858.1:p.Glu2680Ter
XM_011517557.1:c.6247G>T XP_011515859.1:p.Glu2083Ter
XM_011517558.1:c.5797G>T XP_011515860.1:p.Glu1933Ter
XM_011517559.1:c.5005G>T XP_011515861.1:p.Glu1669Ter
XM_011517553.2:c.8260G>T XP_011515855.1:p.Glu2754Ter
XM_011517554.3:c.8260G>T XP_011515856.1:p.Glu2754Ter
XM_011517555.2:c.8257G>T XP_011515857.1:p.Glu2753Ter
XM_017013612.1:c.8260G>T XP_016869101.1:p.Glu2754Ter
XM_017013613.1:c.8167G>T XP_016869102.1:p.Glu2723Ter
NM_017780.4:c.8170G>T MANE Select NP_060250.2:p.Glu2724Ter