Canonical Allele Identifier: CA2479117630

Gene: PRPF3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150346671T= , CM000663.2:g.150346671T=	GRCh38
NC_000001.10:g.150319147T= , CM000663.1:g.150319147T=	GRCh37
NC_000001.9:g.148585771T=	NCBI36
NG_008245.1:g.30220T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324862.7:c.1843+180T= MANE Select	ENSP00000315379.6:n.1843+180T=
ENST00000324862.6:c.1843+180T=	ENSP00000315379.6:n.1843+180T=
ENST00000467329.5:n.2170+180T=
ENST00000476970.1:n.952+180T=
NM_004698.2:c.1843+180T=	NP_004689.1:n.1843+180T=
XM_011510128.1:c.1853+170T=	XP_011508430.1:n.1853+170T=
XM_011510129.1:c.1438+180T=	XP_011508431.1:n.1438+180T=
XM_011510130.1:c.1411+180T=	XP_011508432.1:n.1411+180T=
XR_241103.1:n.1826+180T=
XR_921997.1:n.1836+170T=
XR_921998.1:n.1940+180T=
NM_001350529.1:c.1438+180T=	NP_001337458.1:n.1438+180T=
NM_004698.3:c.1843+180T=	NP_004689.1:n.1843+180T=
NR_146766.1:n.2074+180T=
NR_146767.1:n.2170+180T=
NR_146768.1:n.2026+170T=
NR_146769.1:n.2079+170T=
XM_011510130.3:c.1411+180T=	XP_011508432.1:n.1411+180T=
XM_017002790.1:c.1411+180T=	XP_016858279.1:n.1411+180T=
XR_001737536.2:n.1876+180T=
XR_001737537.2:n.1990+180T=
XR_001737540.2:n.2747+180T=
XR_001737541.2:n.1770+180T=
XR_002958009.1:n.2500+180T=
XR_002958010.1:n.3746+170T=
XR_002958012.1:n.1942+170T=
XR_241103.3:n.1818+180T=
XR_921997.3:n.1828+170T=
XR_921998.3:n.1932+180T=
NM_004698.4:c.1843+180T= MANE Select	NP_004689.1:n.1843+180T=