Canonical Allele Identifier: CA371321316

Gene: CHD7

Linked Data

• ClinVar Variation Id: 2807324
• ClinVar RCV Id: RCV003604117
• dbSNP Id: rs1805341017
• MyVariant Identifiers: chr8:g.61761702T>C (hg19) ; chr8:g.60849143T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60849143T>C , CM000670.2:g.60849143T>C	GRCh38
NC_000008.10:g.61761702T>C , CM000670.1:g.61761702T>C	GRCh37
NC_000008.9:g.61924256T>C	NCBI36
NG_007009.1:g.175364T>C , LRG_176:g.175364T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695853.1:c.5393T>C	ENSP00000512218.1:p.Val1798Ala
ENST00000423902.7:c.5393T>C MANE Select	ENSP00000392028.1:p.Val1798Ala
ENST00000423902.6:c.5393T>C	ENSP00000392028.1:p.Val1798Ala
ENST00000524602.5:c.1717-13086T>C	ENSP00000437061.1:n.1717-13086T>C
NM_001316690.1:c.1717-13086T>C	NP_001303619.1:n.1717-13086T>C
NM_017780.3:c.5393T>C	NP_060250.2:p.Val1798Ala
XM_011517553.1:c.5483T>C	XP_011515855.1:p.Val1828Ala
XM_011517554.1:c.5483T>C	XP_011515856.1:p.Val1828Ala
XM_011517555.1:c.5483T>C	XP_011515857.1:p.Val1828Ala
XM_011517556.1:c.5483T>C	XP_011515858.1:p.Val1828Ala
XM_011517557.1:c.3470T>C	XP_011515859.1:p.Val1157Ala
XM_011517558.1:c.3020T>C	XP_011515860.1:p.Val1007Ala
XM_011517559.1:c.2228T>C	XP_011515861.1:p.Val743Ala
XM_011517553.2:c.5483T>C	XP_011515855.1:p.Val1828Ala
XM_011517554.3:c.5483T>C	XP_011515856.1:p.Val1828Ala
XM_011517555.2:c.5483T>C	XP_011515857.1:p.Val1828Ala
XM_017013612.1:c.5483T>C	XP_016869101.1:p.Val1828Ala
XM_017013613.1:c.5393T>C	XP_016869102.1:p.Val1798Ala
NM_017780.4:c.5393T>C MANE Select	NP_060250.2:p.Val1798Ala