Canonical Allele Identifier: CA371307438

Gene: CHD7

Linked Data

• MyVariant Identifiers: chr8:g.61777660C>A (hg19) ; chr8:g.60865101C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60865101C>A , CM000670.2:g.60865101C>A	GRCh38
NC_000008.10:g.61777660C>A , CM000670.1:g.61777660C>A	GRCh37
NC_000008.9:g.61940214C>A	NCBI36
NG_007009.1:g.191322C>A , LRG_176:g.191322C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.1338C>A
ENST00000695852.1:n.269C>A
ENST00000695853.1:c.*1221C>A	ENSP00000512218.1:n.*1221C>A
ENST00000423902.7:c.8162C>A MANE Select	ENSP00000392028.1:p.Pro2721His
ENST00000423902.6:c.8162C>A	ENSP00000392028.1:p.Pro2721His
ENST00000524602.5:c.2015C>A	ENSP00000437061.1:p.Pro672His
ENST00000528280.1:n.208C>A
ENST00000532149.1:n.584C>A
ENST00000618450.1:n.4198C>A
NM_001316690.1:c.2015C>A	NP_001303619.1:p.Pro672His
NM_017780.3:c.8162C>A	NP_060250.2:p.Pro2721His
XM_011517553.1:c.8252C>A	XP_011515855.1:p.Pro2751His
XM_011517554.1:c.8252C>A	XP_011515856.1:p.Pro2751His
XM_011517555.1:c.8249C>A	XP_011515857.1:p.Pro2750His
XM_011517556.1:c.8030C>A	XP_011515858.1:p.Pro2677His
XM_011517557.1:c.6239C>A	XP_011515859.1:p.Pro2080His
XM_011517558.1:c.5789C>A	XP_011515860.1:p.Pro1930His
XM_011517559.1:c.4997C>A	XP_011515861.1:p.Pro1666His
XM_011517553.2:c.8252C>A	XP_011515855.1:p.Pro2751His
XM_011517554.3:c.8252C>A	XP_011515856.1:p.Pro2751His
XM_011517555.2:c.8249C>A	XP_011515857.1:p.Pro2750His
XM_017013612.1:c.8252C>A	XP_016869101.1:p.Pro2751His
XM_017013613.1:c.8159C>A	XP_016869102.1:p.Pro2720His
NM_017780.4:c.8162C>A MANE Select	NP_060250.2:p.Pro2721His