Canonical Allele Identifier: CA371324995

Gene: CHD7

Linked Data

• MyVariant Identifiers: chr8:g.61765670A>T (hg19) ; chr8:g.60853111A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60853111A>T , CM000670.2:g.60853111A>T	GRCh38
NC_000008.10:g.61765670A>T , CM000670.1:g.61765670A>T	GRCh37
NC_000008.9:g.61928224A>T	NCBI36
NG_007009.1:g.179332A>T , LRG_176:g.179332A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695853.1:c.6386A>T	ENSP00000512218.1:p.Lys2129Ile
ENST00000423902.7:c.6386A>T MANE Select	ENSP00000392028.1:p.Lys2129Ile
ENST00000423902.6:c.6386A>T	ENSP00000392028.1:p.Lys2129Ile
ENST00000524602.5:c.1717-9118A>T	ENSP00000437061.1:n.1717-9118A>T
NM_001316690.1:c.1717-9118A>T	NP_001303619.1:n.1717-9118A>T
NM_017780.3:c.6386A>T	NP_060250.2:p.Lys2129Ile
XM_011517553.1:c.6476A>T	XP_011515855.1:p.Lys2159Ile
XM_011517554.1:c.6476A>T	XP_011515856.1:p.Lys2159Ile
XM_011517555.1:c.6476A>T	XP_011515857.1:p.Lys2159Ile
XM_011517556.1:c.6476A>T	XP_011515858.1:p.Lys2159Ile
XM_011517557.1:c.4463A>T	XP_011515859.1:p.Lys1488Ile
XM_011517558.1:c.4013A>T	XP_011515860.1:p.Lys1338Ile
XM_011517559.1:c.3221A>T	XP_011515861.1:p.Lys1074Ile
XM_011517553.2:c.6476A>T	XP_011515855.1:p.Lys2159Ile
XM_011517554.3:c.6476A>T	XP_011515856.1:p.Lys2159Ile
XM_011517555.2:c.6476A>T	XP_011515857.1:p.Lys2159Ile
XM_017013612.1:c.6476A>T	XP_016869101.1:p.Lys2159Ile
XM_017013613.1:c.6386A>T	XP_016869102.1:p.Lys2129Ile
NM_017780.4:c.6386A>T MANE Select	NP_060250.2:p.Lys2129Ile