Canonical Allele Identifier: CA2635248904

Gene: PRPF8

Linked Data

• gnomAD v4: 17-1651031-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1651033del , CM000679.2:g.1651033del	GRCh38
NC_000017.10:g.1554327del , CM000679.1:g.1554327del	GRCh37
NC_000017.9:g.1501077del	NCBI36
NG_009118.1:g.38851del
NG_033061.1:g.4067del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000573725.2:c.6674-76del	ENSP00000460849.2:n.6674-76del
ENST00000703537.1:c.2602-76del
ENST00000703538.1:c.*6577-76del	ENSP00000515361.1:n.*6577-76del
ENST00000703539.1:n.3168-76del
ENST00000703540.1:c.6707-76del	ENSP00000515362.1:n.6707-76del
ENST00000703541.1:c.6719-76del	ENSP00000515363.1:n.6719-76del
ENST00000304992.11:c.6854-76del MANE Select	ENSP00000304350.6:n.6854-76del
ENST00000304992.10:c.6854-76del	ENSP00000304350.6:n.6854-76del
ENST00000571958.1:c.162+76del
ENST00000572621.5:c.6854-76del	ENSP00000460348.1:n.6854-76del
ENST00000572723.1:n.843-76del
NM_006445.3:c.6854-76del	NP_006436.3:n.6854-76del
XM_024450537.1:c.6854-76del	XP_024306305.1:n.6854-76del
NM_006445.4:c.6854-76del MANE Select	NP_006436.3:n.6854-76del