Canonical Allele Identifier: CA371307537

Gene: CHD7

Linked Data

• MyVariant Identifiers: chr8:g.61777672T>C (hg19) ; chr8:g.60865113T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60865113T>C , CM000670.2:g.60865113T>C	GRCh38
NC_000008.10:g.61777672T>C , CM000670.1:g.61777672T>C	GRCh37
NC_000008.9:g.61940226T>C	NCBI36
NG_007009.1:g.191334T>C , LRG_176:g.191334T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.1350T>C
ENST00000695852.1:n.281T>C
ENST00000695853.1:c.*1233T>C	ENSP00000512218.1:n.*1233T>C
ENST00000423902.7:c.8174T>C MANE Select	ENSP00000392028.1:p.Ile2725Thr
ENST00000423902.6:c.8174T>C	ENSP00000392028.1:p.Ile2725Thr
ENST00000524602.5:c.2027T>C	ENSP00000437061.1:p.Ile676Thr
ENST00000528280.1:n.220T>C
ENST00000532149.1:n.596T>C
ENST00000618450.1:n.4210T>C
NM_001316690.1:c.2027T>C	NP_001303619.1:p.Ile676Thr
NM_017780.3:c.8174T>C	NP_060250.2:p.Ile2725Thr
XM_011517553.1:c.8264T>C	XP_011515855.1:p.Ile2755Thr
XM_011517554.1:c.8264T>C	XP_011515856.1:p.Ile2755Thr
XM_011517555.1:c.8261T>C	XP_011515857.1:p.Ile2754Thr
XM_011517556.1:c.8042T>C	XP_011515858.1:p.Ile2681Thr
XM_011517557.1:c.6251T>C	XP_011515859.1:p.Ile2084Thr
XM_011517558.1:c.5801T>C	XP_011515860.1:p.Ile1934Thr
XM_011517559.1:c.5009T>C	XP_011515861.1:p.Ile1670Thr
XM_011517553.2:c.8264T>C	XP_011515855.1:p.Ile2755Thr
XM_011517554.3:c.8264T>C	XP_011515856.1:p.Ile2755Thr
XM_011517555.2:c.8261T>C	XP_011515857.1:p.Ile2754Thr
XM_017013612.1:c.8264T>C	XP_016869101.1:p.Ile2755Thr
XM_017013613.1:c.8171T>C	XP_016869102.1:p.Ile2724Thr
NM_017780.4:c.8174T>C MANE Select	NP_060250.2:p.Ile2725Thr