Canonical Allele Identifier: CA460845365

Gene: CHD7

Linked Data

• MyVariant Identifiers: chr8:g.61729015T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60816456T>C , CM000670.2:g.60816456T>C	GRCh38
NC_000008.10:g.61729015T>C , CM000670.1:g.61729015T>C	GRCh37
NC_000008.9:g.61891569T>C	NCBI36
NG_007009.1:g.142677T>C , LRG_176:g.142677T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000695853.1:c.2568T>C	ENSP00000512218.1:p.Ile856=
ENST00000423902.7:c.2568T>C MANE Select	ENSP00000392028.1:p.Ile856=
ENST00000423902.6:c.2568T>C	ENSP00000392028.1:p.Ile856=
ENST00000524602.5:c.1716+35406T>C	ENSP00000437061.1:n.1716+35406T>C
ENST00000525508.1:c.2568T>C	ENSP00000436027.1:p.Ile856=
NM_001316690.1:c.1716+35406T>C	NP_001303619.1:n.1716+35406T>C
NM_017780.3:c.2568T>C	NP_060250.2:p.Ile856=
XM_011517553.1:c.2568T>C	XP_011515855.1:p.Ile856=
XM_011517554.1:c.2568T>C	XP_011515856.1:p.Ile856=
XM_011517555.1:c.2568T>C	XP_011515857.1:p.Ile856=
XM_011517556.1:c.2568T>C	XP_011515858.1:p.Ile856=
XM_011517557.1:c.555T>C	XP_011515859.1:p.Ile185=
XM_011517558.1:c.105T>C	XP_011515860.1:p.Ile35=
XM_011517560.1:c.2568T>C	XP_011515862.1:p.Ile856=
XM_011517553.2:c.2568T>C	XP_011515855.1:p.Ile856=
XM_011517554.3:c.2568T>C	XP_011515856.1:p.Ile856=
XM_011517555.2:c.2568T>C	XP_011515857.1:p.Ile856=
XM_011517560.2:c.2568T>C	XP_011515862.1:p.Ile856=
XM_017013612.1:c.2568T>C	XP_016869101.1:p.Ile856=
XM_017013613.1:c.2568T>C	XP_016869102.1:p.Ile856=
NM_017780.4:c.2568T>C MANE Select	NP_060250.2:p.Ile856=