Canonical Allele Identifier: CA401144180

Gene: QRICH2

Linked Data

• MyVariant Identifiers: chr17:g.74283882T>A (hg19) ; chr17:g.76287801T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76287801T>A , CM000679.2:g.76287801T>A	GRCh38
NC_000017.10:g.74283882T>A , CM000679.1:g.74283882T>A	GRCh37
NC_000017.9:g.71795477T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000680821.2:c.3895A>T MANE Select	ENSP00000504874.1:p.Arg1299Ter
ENST00000262765.10:c.3397A>T	ENSP00000262765.5:p.Arg1133Ter
ENST00000636395.1:c.3895A>T	ENSP00000490761.1:p.Arg1299Ter
ENST00000680821.1:c.3895A>T	ENSP00000504874.1:p.Arg1299Ter
ENST00000262765.9:c.3397A>T	ENSP00000262765.5:p.Arg1133Ter
ENST00000447564.2:c.421A>T	ENSP00000394461.2:p.Arg141Ter
ENST00000524722.1:c.*161A>T	ENSP00000432679.1:n.*161A>T
NM_032134.2:c.3397A>T	NP_115510.1:p.Arg1133Ter
NR_130649.1:n.668A>T
XM_005257728.2:c.3895A>T	XP_005257785.1:p.Arg1299Ter
XM_006722136.2:c.157A>T	XP_006722199.1:p.Arg53Ter
XM_011525344.1:c.3175A>T	XP_011523646.1:p.Arg1059Ter
XM_005257728.4:c.3895A>T	XP_005257785.1:p.Arg1299Ter
XM_006722136.3:c.157A>T	XP_006722199.1:p.Arg53Ter
XM_011525344.2:c.3175A>T	XP_011523646.1:p.Arg1059Ter
XM_017025206.2:c.3895A>T	XP_016880695.1:p.Arg1299Ter
XM_017025207.2:c.3835A>T	XP_016880696.1:p.Arg1279Ter
XM_017025208.1:c.-72A>T	XP_016880697.1:n.-72A>T
NM_001388453.1:c.3895A>T MANE Select	NP_001375382.1:p.Arg1299Ter
NM_032134.3:c.3895A>T	NP_115510.2:p.Arg1299Ter
NR_130649.2:n.1264A>T