Canonical Allele Identifier: CA2275923759

Gene: QRICH2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76287731C= , CM000679.2:g.76287731C=	GRCh38
NC_000017.10:g.74283812C= , CM000679.1:g.74283812C=	GRCh37
NC_000017.9:g.71795407C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000680821.2:c.3896+69G= MANE Select	ENSP00000504874.1:n.3896+69G=
ENST00000262765.10:c.3398+69G=	ENSP00000262765.5:n.3398+69G=
ENST00000636395.1:c.3896+69G=	ENSP00000490761.1:n.3896+69G=
ENST00000680821.1:c.3896+69G=	ENSP00000504874.1:n.3896+69G=
ENST00000262765.9:c.3398+69G=	ENSP00000262765.5:n.3398+69G=
ENST00000447564.2:c.422+69G=	ENSP00000394461.2:n.422+69G=
ENST00000524722.1:c.*162+69G=	ENSP00000432679.1:n.*162+69G=
NM_032134.2:c.3398+69G=	NP_115510.1:n.3398+69G=
NR_130649.1:n.669+69G=
XM_005257728.2:c.3896+69G=	XP_005257785.1:n.3896+69G=
XM_006722136.2:c.158+69G=	XP_006722199.1:n.158+69G=
XM_011525344.1:c.3176+69G=	XP_011523646.1:n.3176+69G=
XM_005257728.4:c.3896+69G=	XP_005257785.1:n.3896+69G=
XM_006722136.3:c.158+69G=	XP_006722199.1:n.158+69G=
XM_011525344.2:c.3176+69G=	XP_011523646.1:n.3176+69G=
XM_017025206.2:c.3896+69G=	XP_016880695.1:n.3896+69G=
XM_017025207.2:c.3836+69G=	XP_016880696.1:n.3836+69G=
XM_017025208.1:c.-71+69G=	XP_016880697.1:n.-71+69G=
NM_001388453.1:c.3896+69G= MANE Select	NP_001375382.1:n.3896+69G=
NM_032134.3:c.3896+69G=	NP_115510.2:n.3896+69G=
NR_130649.2:n.1265+69G=