Canonical Allele Identifier: CA30028336
Gene: PRPF3 HGNC NCBI

Linked Data

dbSNP Id: rs201979121

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.150346598_150346601dup , CM000663.2:g.150346598_150346601dup GRCh38
NC_000001.10:g.150319074_150319077dup , CM000663.1:g.150319074_150319077dup GRCh37
NC_000001.9:g.148585698_148585701dup NCBI36
NG_008245.1:g.30147_30150dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000324862.7:c.1843+107_1843+110dup MANE Select ENSP00000315379.6:n.1843+107_1843+110dup
ENST00000324862.6:c.1843+107_1843+110dup ENSP00000315379.6:n.1843+107_1843+110dup
ENST00000467329.5:n.2170+107_2170+110dup
ENST00000476970.1:n.952+107_952+110dup
NM_004698.2:c.1843+107_1843+110dup NP_004689.1:n.1843+107_1843+110dup
XM_011510128.1:c.1853+97_1853+100dup XP_011508430.1:n.1853+97_1853+100dup
XM_011510129.1:c.1438+107_1438+110dup XP_011508431.1:n.1438+107_1438+110dup
XM_011510130.1:c.1411+107_1411+110dup XP_011508432.1:n.1411+107_1411+110dup
XR_241103.1:n.1826+107_1826+110dup
XR_921997.1:n.1836+97_1836+100dup
XR_921998.1:n.1940+107_1940+110dup
NM_001350529.1:c.1438+107_1438+110dup NP_001337458.1:n.1438+107_1438+110dup
NM_004698.3:c.1843+107_1843+110dup NP_004689.1:n.1843+107_1843+110dup
NR_146766.1:n.2074+107_2074+110dup
NR_146767.1:n.2170+107_2170+110dup
NR_146768.1:n.2026+97_2026+100dup
NR_146769.1:n.2079+97_2079+100dup
XM_011510130.3:c.1411+107_1411+110dup XP_011508432.1:n.1411+107_1411+110dup
XM_017002790.1:c.1411+107_1411+110dup XP_016858279.1:n.1411+107_1411+110dup
XR_001737536.2:n.1876+107_1876+110dup
XR_001737537.2:n.1990+107_1990+110dup
XR_001737540.2:n.2747+107_2747+110dup
XR_001737541.2:n.1770+107_1770+110dup
XR_002958009.1:n.2500+107_2500+110dup
XR_002958010.1:n.3746+97_3746+100dup
XR_002958012.1:n.1942+97_1942+100dup
XR_241103.3:n.1818+107_1818+110dup
XR_921997.3:n.1828+97_1828+100dup
XR_921998.3:n.1932+107_1932+110dup
NM_004698.4:c.1843+107_1843+110dup MANE Select NP_004689.1:n.1843+107_1843+110dup