Canonical Allele Identifier: CA371309819

Gene: CHD7

Linked Data

• MyVariant Identifiers: chr8:g.61777983A>G (hg19) ; chr8:g.60865424A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60865424A>G , CM000670.2:g.60865424A>G	GRCh38
NC_000008.10:g.61777983A>G , CM000670.1:g.61777983A>G	GRCh37
NC_000008.9:g.61940537A>G	NCBI36
NG_007009.1:g.191645A>G , LRG_176:g.191645A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.1661A>G
ENST00000695852.1:n.592A>G
ENST00000695853.1:c.*1544A>G	ENSP00000512218.1:n.*1544A>G
ENST00000423902.7:c.8485A>G MANE Select	ENSP00000392028.1:p.Thr2829Ala
ENST00000423902.6:c.8485A>G	ENSP00000392028.1:p.Thr2829Ala
ENST00000524602.5:c.2338A>G	ENSP00000437061.1:p.Thr780Ala
ENST00000528280.1:n.531A>G
NM_001316690.1:c.2338A>G	NP_001303619.1:p.Thr780Ala
NM_017780.3:c.8485A>G	NP_060250.2:p.Thr2829Ala
XM_011517553.1:c.8575A>G	XP_011515855.1:p.Thr2859Ala
XM_011517554.1:c.8575A>G	XP_011515856.1:p.Thr2859Ala
XM_011517555.1:c.8572A>G	XP_011515857.1:p.Thr2858Ala
XM_011517556.1:c.8353A>G	XP_011515858.1:p.Thr2785Ala
XM_011517557.1:c.6562A>G	XP_011515859.1:p.Thr2188Ala
XM_011517558.1:c.6112A>G	XP_011515860.1:p.Thr2038Ala
XM_011517559.1:c.5320A>G	XP_011515861.1:p.Thr1774Ala
XM_011517553.2:c.8575A>G	XP_011515855.1:p.Thr2859Ala
XM_011517554.3:c.8575A>G	XP_011515856.1:p.Thr2859Ala
XM_011517555.2:c.8572A>G	XP_011515857.1:p.Thr2858Ala
XM_017013612.1:c.8575A>G	XP_016869101.1:p.Thr2859Ala
XM_017013613.1:c.8482A>G	XP_016869102.1:p.Thr2828Ala
NM_017780.4:c.8485A>G MANE Select	NP_060250.2:p.Thr2829Ala