Canonical Allele Identifier: CA371304136

Gene: CHD7

Linked Data

• MyVariant Identifiers: chr8:g.61773469G>C (hg19) ; chr8:g.60860910G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60860910G>C , CM000670.2:g.60860910G>C	GRCh38
NC_000008.10:g.61773469G>C , CM000670.1:g.61773469G>C	GRCh37
NC_000008.9:g.61936023G>C	NCBI36
NG_007009.1:g.187131G>C , LRG_176:g.187131G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.791G>C
ENST00000695853.1:c.*674G>C	ENSP00000512218.1:n.*674G>C
ENST00000423902.7:c.7615G>C MANE Select	ENSP00000392028.1:p.Ala2539Pro
ENST00000423902.6:c.7615G>C	ENSP00000392028.1:p.Ala2539Pro
ENST00000524602.5:c.1717-1319G>C	ENSP00000437061.1:n.1717-1319G>C
ENST00000531695.1:n.39G>C
ENST00000618450.1:n.7G>C
NM_001316690.1:c.1717-1319G>C	NP_001303619.1:n.1717-1319G>C
NM_017780.3:c.7615G>C	NP_060250.2:p.Ala2539Pro
XM_011517553.1:c.7705G>C	XP_011515855.1:p.Ala2569Pro
XM_011517554.1:c.7705G>C	XP_011515856.1:p.Ala2569Pro
XM_011517555.1:c.7702G>C	XP_011515857.1:p.Ala2568Pro
XM_011517556.1:c.7699-1286G>C	XP_011515858.1:n.7699-1286G>C
XM_011517557.1:c.5692G>C	XP_011515859.1:p.Ala1898Pro
XM_011517558.1:c.5242G>C	XP_011515860.1:p.Ala1748Pro
XM_011517559.1:c.4450G>C	XP_011515861.1:p.Ala1484Pro
XM_011517553.2:c.7705G>C	XP_011515855.1:p.Ala2569Pro
XM_011517554.3:c.7705G>C	XP_011515856.1:p.Ala2569Pro
XM_011517555.2:c.7702G>C	XP_011515857.1:p.Ala2568Pro
XM_017013612.1:c.7705G>C	XP_016869101.1:p.Ala2569Pro
XM_017013613.1:c.7612G>C	XP_016869102.1:p.Ala2538Pro
NM_017780.4:c.7615G>C MANE Select	NP_060250.2:p.Ala2539Pro