Canonical Allele Identifier: CA461104147

Gene: CHD7

Linked Data

• MyVariant Identifiers: chr8:g.61693591A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60781032A>C , CM000670.2:g.60781032A>C	GRCh38
NC_000008.10:g.61693591A>C , CM000670.1:g.61693591A>C	GRCh37
NC_000008.9:g.61856145A>C	NCBI36
NG_007009.1:g.107253A>C , LRG_176:g.107253A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000695848.1:n.2211A>C
ENST00000695849.1:n.2211A>C
ENST00000695853.1:c.1698A>C	ENSP00000512218.1:p.Pro566=
ENST00000700671.1:c.1698A>C	ENSP00000515139.1:p.Pro566=
ENST00000423902.7:c.1698A>C MANE Select	ENSP00000392028.1:p.Pro566=
ENST00000423902.6:c.1698A>C	ENSP00000392028.1:p.Pro566=
ENST00000524602.5:c.1698A>C	ENSP00000437061.1:p.Pro566=
ENST00000525508.1:c.1698A>C	ENSP00000436027.1:p.Pro566=
ENST00000527825.1:c.342A>C
ENST00000527900.1:c.99A>C	ENSP00000433336.1:p.Pro33=
NM_001316690.1:c.1698A>C	NP_001303619.1:p.Pro566=
NM_017780.3:c.1698A>C	NP_060250.2:p.Pro566=
XM_011517553.1:c.1698A>C	XP_011515855.1:p.Pro566=
XM_011517554.1:c.1698A>C	XP_011515856.1:p.Pro566=
XM_011517555.1:c.1698A>C	XP_011515857.1:p.Pro566=
XM_011517556.1:c.1698A>C	XP_011515858.1:p.Pro566=
XM_011517560.1:c.1698A>C	XP_011515862.1:p.Pro566=
XM_011517553.2:c.1698A>C	XP_011515855.1:p.Pro566=
XM_011517554.3:c.1698A>C	XP_011515856.1:p.Pro566=
XM_011517555.2:c.1698A>C	XP_011515857.1:p.Pro566=
XM_011517560.2:c.1698A>C	XP_011515862.1:p.Pro566=
XM_017013612.1:c.1698A>C	XP_016869101.1:p.Pro566=
XM_017013613.1:c.1698A>C	XP_016869102.1:p.Pro566=
NM_017780.4:c.1698A>C MANE Select	NP_060250.2:p.Pro566=