Canonical Allele Identifier: CA4760619

Gene: CHD7

Linked Data

• dbSNP Id: rs769201064
• ExAC: 8:61765902 A / C
• gnomAD v2: 8-61765902-A-C
• gnomAD v4: 8-60853343-A-C
• MyVariant Identifiers: chr8:g.61765902A>C (hg19) ; chr8:g.60853343A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60853343A>C , CM000670.2:g.60853343A>C	GRCh38
NC_000008.10:g.61765902A>C , CM000670.1:g.61765902A>C	GRCh37
NC_000008.9:g.61928456A>C	NCBI36
NG_007009.1:g.179564A>C , LRG_176:g.179564A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695853.1:c.6618A>C	ENSP00000512218.1:p.Glu2206Asp
ENST00000423902.7:c.6618A>C MANE Select	ENSP00000392028.1:p.Glu2206Asp
ENST00000423902.6:c.6618A>C	ENSP00000392028.1:p.Glu2206Asp
ENST00000524602.5:c.1717-8886A>C	ENSP00000437061.1:n.1717-8886A>C
NM_001316690.1:c.1717-8886A>C	NP_001303619.1:n.1717-8886A>C
NM_017780.3:c.6618A>C	NP_060250.2:p.Glu2206Asp
XM_011517553.1:c.6708A>C	XP_011515855.1:p.Glu2236Asp
XM_011517554.1:c.6708A>C	XP_011515856.1:p.Glu2236Asp
XM_011517555.1:c.6708A>C	XP_011515857.1:p.Glu2236Asp
XM_011517556.1:c.6708A>C	XP_011515858.1:p.Glu2236Asp
XM_011517557.1:c.4695A>C	XP_011515859.1:p.Glu1565Asp
XM_011517558.1:c.4245A>C	XP_011515860.1:p.Glu1415Asp
XM_011517559.1:c.3453A>C	XP_011515861.1:p.Glu1151Asp
XM_011517553.2:c.6708A>C	XP_011515855.1:p.Glu2236Asp
XM_011517554.3:c.6708A>C	XP_011515856.1:p.Glu2236Asp
XM_011517555.2:c.6708A>C	XP_011515857.1:p.Glu2236Asp
XM_017013612.1:c.6708A>C	XP_016869101.1:p.Glu2236Asp
XM_017013613.1:c.6618A>C	XP_016869102.1:p.Glu2206Asp
NM_017780.4:c.6618A>C MANE Select	NP_060250.2:p.Glu2206Asp