Canonical Allele Identifier: CA460846549

Gene: CHD7

Linked Data

• MyVariant Identifiers: chr8:g.61773612T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60861053T>C , CM000670.2:g.60861053T>C	GRCh38
NC_000008.10:g.61773612T>C , CM000670.1:g.61773612T>C	GRCh37
NC_000008.9:g.61936166T>C	NCBI36
NG_007009.1:g.187274T>C , LRG_176:g.187274T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.934T>C
ENST00000695851.1:n.138T>C
ENST00000695853.1:c.*817T>C	ENSP00000512218.1:n.*817T>C
ENST00000423902.7:c.7758T>C MANE Select	ENSP00000392028.1:p.Pro2586=
ENST00000423902.6:c.7758T>C	ENSP00000392028.1:p.Pro2586=
ENST00000524602.5:c.1717-1176T>C	ENSP00000437061.1:n.1717-1176T>C
ENST00000531695.1:n.182T>C
ENST00000618450.1:n.150T>C
NM_001316690.1:c.1717-1176T>C	NP_001303619.1:n.1717-1176T>C
NM_017780.3:c.7758T>C	NP_060250.2:p.Pro2586=
XM_011517553.1:c.7848T>C	XP_011515855.1:p.Pro2616=
XM_011517554.1:c.7848T>C	XP_011515856.1:p.Pro2616=
XM_011517555.1:c.7845T>C	XP_011515857.1:p.Pro2615=
XM_011517556.1:c.7699-1143T>C	XP_011515858.1:n.7699-1143T>C
XM_011517557.1:c.5835T>C	XP_011515859.1:p.Pro1945=
XM_011517558.1:c.5385T>C	XP_011515860.1:p.Pro1795=
XM_011517559.1:c.4593T>C	XP_011515861.1:p.Pro1531=
XM_011517553.2:c.7848T>C	XP_011515855.1:p.Pro2616=
XM_011517554.3:c.7848T>C	XP_011515856.1:p.Pro2616=
XM_011517555.2:c.7845T>C	XP_011515857.1:p.Pro2615=
XM_017013612.1:c.7848T>C	XP_016869101.1:p.Pro2616=
XM_017013613.1:c.7755T>C	XP_016869102.1:p.Pro2585=
NM_017780.4:c.7758T>C MANE Select	NP_060250.2:p.Pro2586=