Canonical Allele Identifier: CA371304362

Gene: CHD7

Linked Data

• MyVariant Identifiers: chr8:g.61773521A>C (hg19) ; chr8:g.60860962A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60860962A>C , CM000670.2:g.60860962A>C	GRCh38
NC_000008.10:g.61773521A>C , CM000670.1:g.61773521A>C	GRCh37
NC_000008.9:g.61936075A>C	NCBI36
NG_007009.1:g.187183A>C , LRG_176:g.187183A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.843A>C
ENST00000695851.1:n.47A>C
ENST00000695853.1:c.*726A>C	ENSP00000512218.1:n.*726A>C
ENST00000423902.7:c.7667A>C MANE Select	ENSP00000392028.1:p.Asn2556Thr
ENST00000423902.6:c.7667A>C	ENSP00000392028.1:p.Asn2556Thr
ENST00000524602.5:c.1717-1267A>C	ENSP00000437061.1:n.1717-1267A>C
ENST00000531695.1:n.91A>C
ENST00000618450.1:n.59A>C
NM_001316690.1:c.1717-1267A>C	NP_001303619.1:n.1717-1267A>C
NM_017780.3:c.7667A>C	NP_060250.2:p.Asn2556Thr
XM_011517553.1:c.7757A>C	XP_011515855.1:p.Asn2586Thr
XM_011517554.1:c.7757A>C	XP_011515856.1:p.Asn2586Thr
XM_011517555.1:c.7754A>C	XP_011515857.1:p.Asn2585Thr
XM_011517556.1:c.7699-1234A>C	XP_011515858.1:n.7699-1234A>C
XM_011517557.1:c.5744A>C	XP_011515859.1:p.Asn1915Thr
XM_011517558.1:c.5294A>C	XP_011515860.1:p.Asn1765Thr
XM_011517559.1:c.4502A>C	XP_011515861.1:p.Asn1501Thr
XM_011517553.2:c.7757A>C	XP_011515855.1:p.Asn2586Thr
XM_011517554.3:c.7757A>C	XP_011515856.1:p.Asn2586Thr
XM_011517555.2:c.7754A>C	XP_011515857.1:p.Asn2585Thr
XM_017013612.1:c.7757A>C	XP_016869101.1:p.Asn2586Thr
XM_017013613.1:c.7664A>C	XP_016869102.1:p.Asn2555Thr
NM_017780.4:c.7667A>C MANE Select	NP_060250.2:p.Asn2556Thr