Canonical Allele Identifier: CA371309915

Gene: CHD7

Linked Data

• MyVariant Identifiers: chr8:g.61777993G>T (hg19) ; chr8:g.60865434G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60865434G>T , CM000670.2:g.60865434G>T	GRCh38
NC_000008.10:g.61777993G>T , CM000670.1:g.61777993G>T	GRCh37
NC_000008.9:g.61940547G>T	NCBI36
NG_007009.1:g.191655G>T , LRG_176:g.191655G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.1671G>T
ENST00000695852.1:n.602G>T
ENST00000695853.1:c.*1554G>T	ENSP00000512218.1:n.*1554G>T
ENST00000423902.7:c.8495G>T MANE Select	ENSP00000392028.1:p.Ser2832Ile
ENST00000423902.6:c.8495G>T	ENSP00000392028.1:p.Ser2832Ile
ENST00000524602.5:c.2348G>T	ENSP00000437061.1:p.Ser783Ile
ENST00000528280.1:n.541G>T
NM_001316690.1:c.2348G>T	NP_001303619.1:p.Ser783Ile
NM_017780.3:c.8495G>T	NP_060250.2:p.Ser2832Ile
XM_011517553.1:c.8585G>T	XP_011515855.1:p.Ser2862Ile
XM_011517554.1:c.8585G>T	XP_011515856.1:p.Ser2862Ile
XM_011517555.1:c.8582G>T	XP_011515857.1:p.Ser2861Ile
XM_011517556.1:c.8363G>T	XP_011515858.1:p.Ser2788Ile
XM_011517557.1:c.6572G>T	XP_011515859.1:p.Ser2191Ile
XM_011517558.1:c.6122G>T	XP_011515860.1:p.Ser2041Ile
XM_011517559.1:c.5330G>T	XP_011515861.1:p.Ser1777Ile
XM_011517553.2:c.8585G>T	XP_011515855.1:p.Ser2862Ile
XM_011517554.3:c.8585G>T	XP_011515856.1:p.Ser2862Ile
XM_011517555.2:c.8582G>T	XP_011515857.1:p.Ser2861Ile
XM_017013612.1:c.8585G>T	XP_016869101.1:p.Ser2862Ile
XM_017013613.1:c.8492G>T	XP_016869102.1:p.Ser2831Ile
NM_017780.4:c.8495G>T MANE Select	NP_060250.2:p.Ser2832Ile