Canonical Allele Identifier: CA2275923748

Gene: QRICH2

Linked Data

• dbSNP Id: rs2070915920
• gnomAD v4: 17-76287696-A-AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76287698_76287699dup , CM000679.2:g.76287698_76287699dup	GRCh38
NC_000017.10:g.74283779_74283780dup , CM000679.1:g.74283779_74283780dup	GRCh37
NC_000017.9:g.71795374_71795375dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000680821.2:c.3896+102_3896+103dup MANE Select	ENSP00000504874.1:n.3896+102_3896+103dup
ENST00000262765.10:c.3398+102_3398+103dup	ENSP00000262765.5:n.3398+102_3398+103dup
ENST00000636395.1:c.3896+102_3896+103dup	ENSP00000490761.1:n.3896+102_3896+103dup
ENST00000680821.1:c.3896+102_3896+103dup	ENSP00000504874.1:n.3896+102_3896+103dup
ENST00000262765.9:c.3398+102_3398+103dup	ENSP00000262765.5:n.3398+102_3398+103dup
ENST00000447564.2:c.422+102_422+103dup	ENSP00000394461.2:n.422+102_422+103dup
ENST00000524722.1:c.*162+102_*162+103dup	ENSP00000432679.1:n.*162+102_*162+103dup
NM_032134.2:c.3398+102_3398+103dup	NP_115510.1:n.3398+102_3398+103dup
NR_130649.1:n.669+102_669+103dup
XM_005257728.2:c.3896+102_3896+103dup	XP_005257785.1:n.3896+102_3896+103dup
XM_006722136.2:c.158+102_158+103dup	XP_006722199.1:n.158+102_158+103dup
XM_011525344.1:c.3176+102_3176+103dup	XP_011523646.1:n.3176+102_3176+103dup
XM_005257728.4:c.3896+102_3896+103dup	XP_005257785.1:n.3896+102_3896+103dup
XM_006722136.3:c.158+102_158+103dup	XP_006722199.1:n.158+102_158+103dup
XM_011525344.2:c.3176+102_3176+103dup	XP_011523646.1:n.3176+102_3176+103dup
XM_017025206.2:c.3896+102_3896+103dup	XP_016880695.1:n.3896+102_3896+103dup
XM_017025207.2:c.3836+102_3836+103dup	XP_016880696.1:n.3836+102_3836+103dup
XM_017025208.1:c.-71+102_-71+103dup	XP_016880697.1:n.-71+102_-71+103dup
NM_001388453.1:c.3896+102_3896+103dup MANE Select	NP_001375382.1:n.3896+102_3896+103dup
NM_032134.3:c.3896+102_3896+103dup	NP_115510.2:n.3896+102_3896+103dup
NR_130649.2:n.1265+102_1265+103dup