Canonical Allele Identifier: CA371310375

Gene: CHD7

Linked Data

• MyVariant Identifiers: chr8:g.61778041A>C (hg19) ; chr8:g.60865482A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60865482A>C , CM000670.2:g.60865482A>C	GRCh38
NC_000008.10:g.61778041A>C , CM000670.1:g.61778041A>C	GRCh37
NC_000008.9:g.61940595A>C	NCBI36
NG_007009.1:g.191703A>C , LRG_176:g.191703A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.1719A>C
ENST00000695852.1:n.650A>C
ENST00000695853.1:c.*1602A>C	ENSP00000512218.1:n.*1602A>C
ENST00000423902.7:c.8543A>C MANE Select	ENSP00000392028.1:p.Asn2848Thr
ENST00000423902.6:c.8543A>C	ENSP00000392028.1:p.Asn2848Thr
ENST00000524602.5:c.2396A>C	ENSP00000437061.1:p.Asn799Thr
NM_001316690.1:c.2396A>C	NP_001303619.1:p.Asn799Thr
NM_017780.3:c.8543A>C	NP_060250.2:p.Asn2848Thr
XM_011517553.1:c.8633A>C	XP_011515855.1:p.Asn2878Thr
XM_011517554.1:c.8633A>C	XP_011515856.1:p.Asn2878Thr
XM_011517555.1:c.8630A>C	XP_011515857.1:p.Asn2877Thr
XM_011517556.1:c.8411A>C	XP_011515858.1:p.Asn2804Thr
XM_011517557.1:c.6620A>C	XP_011515859.1:p.Asn2207Thr
XM_011517558.1:c.6170A>C	XP_011515860.1:p.Asn2057Thr
XM_011517559.1:c.5378A>C	XP_011515861.1:p.Asn1793Thr
XM_011517553.2:c.8633A>C	XP_011515855.1:p.Asn2878Thr
XM_011517554.3:c.8633A>C	XP_011515856.1:p.Asn2878Thr
XM_011517555.2:c.8630A>C	XP_011515857.1:p.Asn2877Thr
XM_017013612.1:c.8633A>C	XP_016869101.1:p.Asn2878Thr
XM_017013613.1:c.8540A>C	XP_016869102.1:p.Asn2847Thr
NM_017780.4:c.8543A>C MANE Select	NP_060250.2:p.Asn2848Thr