Canonical Allele Identifier: CA243783
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 196708
dbSNP Id: rs367615733
gnomAD v2: 8-61766055-C-T
gnomAD v3: 8-60853496-C-T
gnomAD v4: 8-60853496-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.60853496C>T , CM000670.2:g.60853496C>T GRCh38
NC_000008.10:g.61766055C>T , CM000670.1:g.61766055C>T GRCh37
NC_000008.9:g.61928609C>T NCBI36
NG_007009.1:g.179717C>T , LRG_176:g.179717C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000695853.1:c.6771C>T ENSP00000512218.1:p.Pro2257=
ENST00000423902.7:c.6771C>T MANE Select ENSP00000392028.1:p.Pro2257=
ENST00000423902.6:c.6771C>T ENSP00000392028.1:p.Pro2257=
ENST00000524602.5:c.1717-8733C>T ENSP00000437061.1:n.1717-8733C>T
NM_001316690.1:c.1717-8733C>T NP_001303619.1:n.1717-8733C>T
NM_017780.3:c.6771C>T NP_060250.2:p.Pro2257=
XM_011517553.1:c.6861C>T XP_011515855.1:p.Pro2287=
XM_011517554.1:c.6861C>T XP_011515856.1:p.Pro2287=
XM_011517555.1:c.6861C>T XP_011515857.1:p.Pro2287=
XM_011517556.1:c.6861C>T XP_011515858.1:p.Pro2287=
XM_011517557.1:c.4848C>T XP_011515859.1:p.Pro1616=
XM_011517558.1:c.4398C>T XP_011515860.1:p.Pro1466=
XM_011517559.1:c.3606C>T XP_011515861.1:p.Pro1202=
XM_011517553.2:c.6861C>T XP_011515855.1:p.Pro2287=
XM_011517554.3:c.6861C>T XP_011515856.1:p.Pro2287=
XM_011517555.2:c.6861C>T XP_011515857.1:p.Pro2287=
XM_017013612.1:c.6861C>T XP_016869101.1:p.Pro2287=
XM_017013613.1:c.6771C>T XP_016869102.1:p.Pro2257=
NM_017780.4:c.6771C>T MANE Select NP_060250.2:p.Pro2257=