Canonical Allele Identifier: CA2746071809

Gene: PRPF3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150346691A>C , CM000663.2:g.150346691A>C	GRCh38
NC_000001.10:g.150319167A>C , CM000663.1:g.150319167A>C	GRCh37
NC_000001.9:g.148585791A>C	NCBI36
NG_008245.1:g.30240A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324862.7:c.1843+200A>C MANE Select	ENSP00000315379.6:n.1843+200A>C
ENST00000324862.6:c.1843+200A>C	ENSP00000315379.6:n.1843+200A>C
ENST00000467329.5:n.2170+200A>C
ENST00000476970.1:n.952+200A>C
NM_004698.2:c.1843+200A>C	NP_004689.1:n.1843+200A>C
XM_011510128.1:c.1853+190A>C	XP_011508430.1:n.1853+190A>C
XM_011510129.1:c.1438+200A>C	XP_011508431.1:n.1438+200A>C
XM_011510130.1:c.1411+200A>C	XP_011508432.1:n.1411+200A>C
XR_241103.1:n.1826+200A>C
XR_921997.1:n.1836+190A>C
XR_921998.1:n.1940+200A>C
NM_001350529.1:c.1438+200A>C	NP_001337458.1:n.1438+200A>C
NM_004698.3:c.1843+200A>C	NP_004689.1:n.1843+200A>C
NR_146766.1:n.2074+200A>C
NR_146767.1:n.2170+200A>C
NR_146768.1:n.2026+190A>C
NR_146769.1:n.2079+190A>C
XM_011510130.3:c.1411+200A>C	XP_011508432.1:n.1411+200A>C
XM_017002790.1:c.1411+200A>C	XP_016858279.1:n.1411+200A>C
XR_001737536.2:n.1876+200A>C
XR_001737537.2:n.1990+200A>C
XR_001737540.2:n.2747+200A>C
XR_001737541.2:n.1770+200A>C
XR_002958009.1:n.2500+200A>C
XR_002958010.1:n.3746+190A>C
XR_002958012.1:n.1942+190A>C
XR_241103.3:n.1818+200A>C
XR_921997.3:n.1828+190A>C
XR_921998.3:n.1932+200A>C
NM_004698.4:c.1843+200A>C MANE Select	NP_004689.1:n.1843+200A>C