Canonical Allele Identifier: CA371308846

Gene: CHD7

Linked Data

• dbSNP Id: rs774242976
• gnomAD v4: 8-60865317-C-T
• MyVariant Identifiers: chr8:g.61777876C>T (hg19) ; chr8:g.60865317C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60865317C>T , CM000670.2:g.60865317C>T	GRCh38
NC_000008.10:g.61777876C>T , CM000670.1:g.61777876C>T	GRCh37
NC_000008.9:g.61940430C>T	NCBI36
NG_007009.1:g.191538C>T , LRG_176:g.191538C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.1554C>T
ENST00000695852.1:n.485C>T
ENST00000695853.1:c.*1437C>T	ENSP00000512218.1:n.*1437C>T
ENST00000423902.7:c.8378C>T MANE Select	ENSP00000392028.1:p.Ala2793Val
ENST00000423902.6:c.8378C>T	ENSP00000392028.1:p.Ala2793Val
ENST00000524602.5:c.2231C>T	ENSP00000437061.1:p.Ala744Val
ENST00000528280.1:n.424C>T
NM_001316690.1:c.2231C>T	NP_001303619.1:p.Ala744Val
NM_017780.3:c.8378C>T	NP_060250.2:p.Ala2793Val
XM_011517553.1:c.8468C>T	XP_011515855.1:p.Ala2823Val
XM_011517554.1:c.8468C>T	XP_011515856.1:p.Ala2823Val
XM_011517555.1:c.8465C>T	XP_011515857.1:p.Ala2822Val
XM_011517556.1:c.8246C>T	XP_011515858.1:p.Ala2749Val
XM_011517557.1:c.6455C>T	XP_011515859.1:p.Ala2152Val
XM_011517558.1:c.6005C>T	XP_011515860.1:p.Ala2002Val
XM_011517559.1:c.5213C>T	XP_011515861.1:p.Ala1738Val
XM_011517553.2:c.8468C>T	XP_011515855.1:p.Ala2823Val
XM_011517554.3:c.8468C>T	XP_011515856.1:p.Ala2823Val
XM_011517555.2:c.8465C>T	XP_011515857.1:p.Ala2822Val
XM_017013612.1:c.8468C>T	XP_016869101.1:p.Ala2823Val
XM_017013613.1:c.8375C>T	XP_016869102.1:p.Ala2792Val
NM_017780.4:c.8378C>T MANE Select	NP_060250.2:p.Ala2793Val