Canonical Allele Identifier: CA371308681

Gene: CHD7

Linked Data

• ClinVar Variation Id: 666812
• ClinVar RCV Id: RCV000825312
• dbSNP Id: rs373204105
• MyVariant Identifiers: chr8:g.61777860G>C (hg19) ; chr8:g.60865301G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60865301G>C , CM000670.2:g.60865301G>C	GRCh38
NC_000008.10:g.61777860G>C , CM000670.1:g.61777860G>C	GRCh37
NC_000008.9:g.61940414G>C	NCBI36
NG_007009.1:g.191522G>C , LRG_176:g.191522G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.1538G>C
ENST00000695852.1:n.469G>C
ENST00000695853.1:c.*1421G>C	ENSP00000512218.1:n.*1421G>C
ENST00000423902.7:c.8362G>C MANE Select	ENSP00000392028.1:p.Asp2788His
ENST00000423902.6:c.8362G>C	ENSP00000392028.1:p.Asp2788His
ENST00000524602.5:c.2215G>C	ENSP00000437061.1:p.Asp739His
ENST00000528280.1:n.408G>C
NM_001316690.1:c.2215G>C	NP_001303619.1:p.Asp739His
NM_017780.3:c.8362G>C	NP_060250.2:p.Asp2788His
XM_011517553.1:c.8452G>C	XP_011515855.1:p.Asp2818His
XM_011517554.1:c.8452G>C	XP_011515856.1:p.Asp2818His
XM_011517555.1:c.8449G>C	XP_011515857.1:p.Asp2817His
XM_011517556.1:c.8230G>C	XP_011515858.1:p.Asp2744His
XM_011517557.1:c.6439G>C	XP_011515859.1:p.Asp2147His
XM_011517558.1:c.5989G>C	XP_011515860.1:p.Asp1997His
XM_011517559.1:c.5197G>C	XP_011515861.1:p.Asp1733His
XM_011517553.2:c.8452G>C	XP_011515855.1:p.Asp2818His
XM_011517554.3:c.8452G>C	XP_011515856.1:p.Asp2818His
XM_011517555.2:c.8449G>C	XP_011515857.1:p.Asp2817His
XM_017013612.1:c.8452G>C	XP_016869101.1:p.Asp2818His
XM_017013613.1:c.8359G>C	XP_016869102.1:p.Asp2787His
NM_017780.4:c.8362G>C MANE Select	NP_060250.2:p.Asp2788His