Canonical Allele Identifier: CA371324824

Gene: CHD7

Linked Data

• MyVariant Identifiers: chr8:g.61765619C>A (hg19) ; chr8:g.60853060C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60853060C>A , CM000670.2:g.60853060C>A	GRCh38
NC_000008.10:g.61765619C>A , CM000670.1:g.61765619C>A	GRCh37
NC_000008.9:g.61928173C>A	NCBI36
NG_007009.1:g.179281C>A , LRG_176:g.179281C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000695853.1:c.6335C>A	ENSP00000512218.1:p.Thr2112Lys
ENST00000423902.7:c.6335C>A MANE Select	ENSP00000392028.1:p.Thr2112Lys
ENST00000423902.6:c.6335C>A	ENSP00000392028.1:p.Thr2112Lys
ENST00000524602.5:c.1717-9169C>A	ENSP00000437061.1:n.1717-9169C>A
NM_001316690.1:c.1717-9169C>A	NP_001303619.1:n.1717-9169C>A
NM_017780.3:c.6335C>A	NP_060250.2:p.Thr2112Lys
XM_011517553.1:c.6425C>A	XP_011515855.1:p.Thr2142Lys
XM_011517554.1:c.6425C>A	XP_011515856.1:p.Thr2142Lys
XM_011517555.1:c.6425C>A	XP_011515857.1:p.Thr2142Lys
XM_011517556.1:c.6425C>A	XP_011515858.1:p.Thr2142Lys
XM_011517557.1:c.4412C>A	XP_011515859.1:p.Thr1471Lys
XM_011517558.1:c.3962C>A	XP_011515860.1:p.Thr1321Lys
XM_011517559.1:c.3170C>A	XP_011515861.1:p.Thr1057Lys
XM_011517553.2:c.6425C>A	XP_011515855.1:p.Thr2142Lys
XM_011517554.3:c.6425C>A	XP_011515856.1:p.Thr2142Lys
XM_011517555.2:c.6425C>A	XP_011515857.1:p.Thr2142Lys
XM_017013612.1:c.6425C>A	XP_016869101.1:p.Thr2142Lys
XM_017013613.1:c.6335C>A	XP_016869102.1:p.Thr2112Lys
NM_017780.4:c.6335C>A MANE Select	NP_060250.2:p.Thr2112Lys