Canonical Allele Identifier: CA2479116685
Gene: PRPF3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.150344156C= , CM000663.2:g.150344156C= GRCh38
NC_000001.10:g.150316632C= , CM000663.1:g.150316632C= GRCh37
NC_000001.9:g.148583256C= NCBI36
NG_008245.1:g.27705C=

Transcript Alleles

HGVS Amino-acid change
ENST00000324862.7:c.1427-6C= MANE Select ENSP00000315379.6:n.1427-6C=
ENST00000324862.6:c.1427-6C= ENSP00000315379.6:n.1427-6C=
ENST00000467329.5:n.1696-6C=
ENST00000493553.1:n.303-6C=
NM_004698.2:c.1427-6C= NP_004689.1:n.1427-6C=
XM_011510128.1:c.1427-6C= XP_011508430.1:n.1427-6C=
XM_011510129.1:c.1022-6C= XP_011508431.1:n.1022-6C=
XM_011510130.1:c.995-6C= XP_011508432.1:n.995-6C=
XR_241103.1:n.1529-6C=
XR_241104.1:n.1529-6C=
XR_921997.1:n.1529-6C=
XR_921998.1:n.1524-6C=
NM_001350529.1:c.1022-6C= NP_001337458.1:n.1022-6C=
NM_004698.3:c.1427-6C= NP_004689.1:n.1427-6C=
NR_146766.1:n.1600-6C=
NR_146767.1:n.1696-6C=
NR_146768.1:n.1600-6C=
NR_146769.1:n.1595-6C=
XM_011510130.3:c.995-6C= XP_011508432.1:n.995-6C=
XM_017002790.1:c.995-6C= XP_016858279.1:n.995-6C=
XR_001737536.2:n.1521-6C=
XR_001737537.2:n.1516-6C=
XR_001737540.2:n.2273-6C=
XR_001737541.2:n.1354-6C=
XR_002958009.1:n.2026-6C=
XR_002958010.1:n.1521-6C=
XR_002958012.1:n.1516-6C=
XR_241103.3:n.1521-6C=
XR_921997.3:n.1521-6C=
XR_921998.3:n.1516-6C=
NM_004698.4:c.1427-6C= MANE Select NP_004689.1:n.1427-6C=