Canonical Allele Identifier: CA8271181

Gene: PRPF8

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1651711C>T , CM000679.2:g.1651711C>T	GRCh38
NC_000017.10:g.1555005C>T , CM000679.1:g.1555005C>T	GRCh37
NC_000017.9:g.1501755C>T	NCBI36
NG_009118.1:g.38172G>A
NG_033061.1:g.3388G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_006445.4:c.6447G>A MANE Select	NP_006436.3:p.Pro2149=
ENST00000304992.11:c.6447G>A MANE Select	ENSP00000304350.6:p.Pro2149=
NM_006445.3:c.6447G>A	NP_006436.3:p.Pro2149=
ENST00000304992.10:c.6447G>A	ENSP00000304350.6:p.Pro2149=
ENST00000572621.5:c.6447G>A	ENSP00000460348.1:p.Pro2149=
ENST00000572723.1:n.436G>A
ENST00000573725.2:c.6267G>A	ENSP00000460849.2:p.Pro2089=
ENST00000575116.1:n.412G>A
ENST00000703537.1:c.2195G>A
ENST00000703538.1:c.*6170G>A	ENSP00000515361.1:n.*6170G>A
ENST00000703539.1:n.2761G>A
ENST00000703540.1:c.6300G>A	ENSP00000515362.1:p.Pro2100=
ENST00000703541.1:c.6312G>A	ENSP00000515363.1:p.Pro2104=
XM_024450537.1:c.6447G>A	XP_024306305.1:p.Pro2149=