Canonical Allele Identifier: CA371307434

Gene: CHD7

Linked Data

• MyVariant Identifiers: chr8:g.61777659C>T (hg19) ; chr8:g.60865100C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60865100C>T , CM000670.2:g.60865100C>T	GRCh38
NC_000008.10:g.61777659C>T , CM000670.1:g.61777659C>T	GRCh37
NC_000008.9:g.61940213C>T	NCBI36
NG_007009.1:g.191321C>T , LRG_176:g.191321C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.1337C>T
ENST00000695852.1:n.268C>T
ENST00000695853.1:c.*1220C>T	ENSP00000512218.1:n.*1220C>T
ENST00000423902.7:c.8161C>T MANE Select	ENSP00000392028.1:p.Pro2721Ser
ENST00000423902.6:c.8161C>T	ENSP00000392028.1:p.Pro2721Ser
ENST00000524602.5:c.2014C>T	ENSP00000437061.1:p.Pro672Ser
ENST00000528280.1:n.207C>T
ENST00000532149.1:n.583C>T
ENST00000618450.1:n.4197C>T
NM_001316690.1:c.2014C>T	NP_001303619.1:p.Pro672Ser
NM_017780.3:c.8161C>T	NP_060250.2:p.Pro2721Ser
XM_011517553.1:c.8251C>T	XP_011515855.1:p.Pro2751Ser
XM_011517554.1:c.8251C>T	XP_011515856.1:p.Pro2751Ser
XM_011517555.1:c.8248C>T	XP_011515857.1:p.Pro2750Ser
XM_011517556.1:c.8029C>T	XP_011515858.1:p.Pro2677Ser
XM_011517557.1:c.6238C>T	XP_011515859.1:p.Pro2080Ser
XM_011517558.1:c.5788C>T	XP_011515860.1:p.Pro1930Ser
XM_011517559.1:c.4996C>T	XP_011515861.1:p.Pro1666Ser
XM_011517553.2:c.8251C>T	XP_011515855.1:p.Pro2751Ser
XM_011517554.3:c.8251C>T	XP_011515856.1:p.Pro2751Ser
XM_011517555.2:c.8248C>T	XP_011515857.1:p.Pro2750Ser
XM_017013612.1:c.8251C>T	XP_016869101.1:p.Pro2751Ser
XM_017013613.1:c.8158C>T	XP_016869102.1:p.Pro2720Ser
NM_017780.4:c.8161C>T MANE Select	NP_060250.2:p.Pro2721Ser