Canonical Allele Identifier: CA501881290

Gene: QRICH2

Linked Data

• MyVariant Identifiers: chr17:g.74283889A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76287808A>T , CM000679.2:g.76287808A>T	GRCh38
NC_000017.10:g.74283889A>T , CM000679.1:g.74283889A>T	GRCh37
NC_000017.9:g.71795484A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000680821.2:c.3888T>A MANE Select	ENSP00000504874.1:p.Gly1296=
ENST00000262765.10:c.3390T>A	ENSP00000262765.5:p.Gly1130=
ENST00000636395.1:c.3888T>A	ENSP00000490761.1:p.Gly1296=
ENST00000680821.1:c.3888T>A	ENSP00000504874.1:p.Gly1296=
ENST00000262765.9:c.3390T>A	ENSP00000262765.5:p.Gly1130=
ENST00000447564.2:c.414T>A	ENSP00000394461.2:p.Gly138=
ENST00000524722.1:c.*154T>A	ENSP00000432679.1:n.*154T>A
NM_032134.2:c.3390T>A	NP_115510.1:p.Gly1130=
NR_130649.1:n.661T>A
XM_005257728.2:c.3888T>A	XP_005257785.1:p.Gly1296=
XM_006722136.2:c.150T>A	XP_006722199.1:p.Gly50=
XM_011525344.1:c.3168T>A	XP_011523646.1:p.Gly1056=
XM_005257728.4:c.3888T>A	XP_005257785.1:p.Gly1296=
XM_006722136.3:c.150T>A	XP_006722199.1:p.Gly50=
XM_011525344.2:c.3168T>A	XP_011523646.1:p.Gly1056=
XM_017025206.2:c.3888T>A	XP_016880695.1:p.Gly1296=
XM_017025207.2:c.3828T>A	XP_016880696.1:p.Gly1276=
XM_017025208.1:c.-79T>A	XP_016880697.1:n.-79T>A
NM_001388453.1:c.3888T>A MANE Select	NP_001375382.1:p.Gly1296=
NM_032134.3:c.3888T>A	NP_115510.2:p.Gly1296=
NR_130649.2:n.1257T>A