Canonical Allele Identifier: CA371304588

Gene: CHD7

Linked Data

• MyVariant Identifiers: chr8:g.61773593T>C (hg19) ; chr8:g.60861034T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60861034T>C , CM000670.2:g.60861034T>C	GRCh38
NC_000008.10:g.61773593T>C , CM000670.1:g.61773593T>C	GRCh37
NC_000008.9:g.61936147T>C	NCBI36
NG_007009.1:g.187255T>C , LRG_176:g.187255T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.915T>C
ENST00000695851.1:n.119T>C
ENST00000695853.1:c.*798T>C	ENSP00000512218.1:n.*798T>C
ENST00000423902.7:c.7739T>C MANE Select	ENSP00000392028.1:p.Leu2580Pro
ENST00000423902.6:c.7739T>C	ENSP00000392028.1:p.Leu2580Pro
ENST00000524602.5:c.1717-1195T>C	ENSP00000437061.1:n.1717-1195T>C
ENST00000531695.1:n.163T>C
ENST00000618450.1:n.131T>C
NM_001316690.1:c.1717-1195T>C	NP_001303619.1:n.1717-1195T>C
NM_017780.3:c.7739T>C	NP_060250.2:p.Leu2580Pro
XM_011517553.1:c.7829T>C	XP_011515855.1:p.Leu2610Pro
XM_011517554.1:c.7829T>C	XP_011515856.1:p.Leu2610Pro
XM_011517555.1:c.7826T>C	XP_011515857.1:p.Leu2609Pro
XM_011517556.1:c.7699-1162T>C	XP_011515858.1:n.7699-1162T>C
XM_011517557.1:c.5816T>C	XP_011515859.1:p.Leu1939Pro
XM_011517558.1:c.5366T>C	XP_011515860.1:p.Leu1789Pro
XM_011517559.1:c.4574T>C	XP_011515861.1:p.Leu1525Pro
XM_011517553.2:c.7829T>C	XP_011515855.1:p.Leu2610Pro
XM_011517554.3:c.7829T>C	XP_011515856.1:p.Leu2610Pro
XM_011517555.2:c.7826T>C	XP_011515857.1:p.Leu2609Pro
XM_017013612.1:c.7829T>C	XP_016869101.1:p.Leu2610Pro
XM_017013613.1:c.7736T>C	XP_016869102.1:p.Leu2579Pro
NM_017780.4:c.7739T>C MANE Select	NP_060250.2:p.Leu2580Pro