Canonical Allele Identifier: CA1140278280

Gene: PRPF3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150351808C= , CM000663.2:g.150351808C=	GRCh38
NC_000001.10:g.150324284C= , CM000663.1:g.150324284C=	GRCh37
NC_000001.9:g.148590908C=	NCBI36
NG_008245.1:g.35357C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324862.7:c.1906-1025C= MANE Select	ENSP00000315379.6:n.1906-1025C=
ENST00000324862.6:c.1906-1025C=	ENSP00000315379.6:n.1906-1025C=
ENST00000467329.5:n.2233-1025C=
ENST00000470824.1:n.536-1025C=
NM_004698.2:c.1906-1025C=	NP_004689.1:n.1906-1025C=
XM_011510129.1:c.1501-1025C=	XP_011508431.1:n.1501-1025C=
XM_011510130.1:c.1474-1025C=	XP_011508432.1:n.1474-1025C=
XR_241103.1:n.1889-1025C=
XR_921998.1:n.2003-1025C=
NM_001350529.1:c.1501-1025C=	NP_001337458.1:n.1501-1025C=
NM_004698.3:c.1906-1025C=	NP_004689.1:n.1906-1025C=
NR_146766.1:n.2137-1025C=
NR_146767.1:n.2233-1025C=
NR_146768.1:n.2089-1025C=
NR_146769.1:n.2142-1025C=
XM_011510130.3:c.1474-1025C=	XP_011508432.1:n.1474-1025C=
XM_017002790.1:c.1474-1025C=	XP_016858279.1:n.1474-1025C=
XR_001737536.2:n.1939-1025C=
XR_001737537.2:n.2053-1025C=
XR_001737540.2:n.2810-1025C=
XR_001737541.2:n.1833-1025C=
XR_002958009.1:n.2563-1025C=
XR_002958010.1:n.3809-1025C=
XR_002958012.1:n.2005-1025C=
XR_241103.3:n.1881-1025C=
XR_921997.3:n.1891-1025C=
XR_921998.3:n.1995-1025C=
NM_004698.4:c.1906-1025C= MANE Select	NP_004689.1:n.1906-1025C=