Canonical Allele Identifier: CA371307874

Gene: CHD7

Linked Data

• MyVariant Identifiers: chr8:g.61777737A>T (hg19) ; chr8:g.60865178A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60865178A>T , CM000670.2:g.60865178A>T	GRCh38
NC_000008.10:g.61777737A>T , CM000670.1:g.61777737A>T	GRCh37
NC_000008.9:g.61940291A>T	NCBI36
NG_007009.1:g.191399A>T , LRG_176:g.191399A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.1415A>T
ENST00000695852.1:n.346A>T
ENST00000695853.1:c.*1298A>T	ENSP00000512218.1:n.*1298A>T
ENST00000423902.7:c.8239A>T MANE Select	ENSP00000392028.1:p.Asn2747Tyr
ENST00000423902.6:c.8239A>T	ENSP00000392028.1:p.Asn2747Tyr
ENST00000524602.5:c.2092A>T	ENSP00000437061.1:p.Asn698Tyr
ENST00000528280.1:n.285A>T
NM_001316690.1:c.2092A>T	NP_001303619.1:p.Asn698Tyr
NM_017780.3:c.8239A>T	NP_060250.2:p.Asn2747Tyr
XM_011517553.1:c.8329A>T	XP_011515855.1:p.Asn2777Tyr
XM_011517554.1:c.8329A>T	XP_011515856.1:p.Asn2777Tyr
XM_011517555.1:c.8326A>T	XP_011515857.1:p.Asn2776Tyr
XM_011517556.1:c.8107A>T	XP_011515858.1:p.Asn2703Tyr
XM_011517557.1:c.6316A>T	XP_011515859.1:p.Asn2106Tyr
XM_011517558.1:c.5866A>T	XP_011515860.1:p.Asn1956Tyr
XM_011517559.1:c.5074A>T	XP_011515861.1:p.Asn1692Tyr
XM_011517553.2:c.8329A>T	XP_011515855.1:p.Asn2777Tyr
XM_011517554.3:c.8329A>T	XP_011515856.1:p.Asn2777Tyr
XM_011517555.2:c.8326A>T	XP_011515857.1:p.Asn2776Tyr
XM_017013612.1:c.8329A>T	XP_016869101.1:p.Asn2777Tyr
XM_017013613.1:c.8236A>T	XP_016869102.1:p.Asn2746Tyr
NM_017780.4:c.8239A>T MANE Select	NP_060250.2:p.Asn2747Tyr