Canonical Allele Identifier: CA624564371

Gene: PRPF8

Linked Data

• dbSNP Id: rs1467838102
• gnomAD v2: 17-1554607-G-C
• gnomAD v4: 17-1651313-G-C
• MyVariant Identifiers: chr17:g.1554607G>C (hg19) ; chr17:g.1651313G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1651313G>C , CM000679.2:g.1651313G>C	GRCh38
NC_000017.10:g.1554607G>C , CM000679.1:g.1554607G>C	GRCh37
NC_000017.9:g.1501357G>C	NCBI36
NG_009118.1:g.38570C>G
NG_033061.1:g.3786C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000573725.2:c.6471-3C>G	ENSP00000460849.2:n.6471-3C>G
ENST00000703537.1:c.2399-3C>G
ENST00000703538.1:c.*6374-3C>G	ENSP00000515361.1:n.*6374-3C>G
ENST00000703539.1:n.2965-3C>G
ENST00000703540.1:c.6504-3C>G	ENSP00000515362.1:n.6504-3C>G
ENST00000703541.1:c.6516-3C>G	ENSP00000515363.1:n.6516-3C>G
ENST00000304992.11:c.6651-3C>G MANE Select	ENSP00000304350.6:n.6651-3C>G
ENST00000304992.10:c.6651-3C>G	ENSP00000304350.6:n.6651-3C>G
ENST00000572621.5:c.6651-3C>G	ENSP00000460348.1:n.6651-3C>G
ENST00000572723.1:n.640-3C>G
NM_006445.3:c.6651-3C>G	NP_006436.3:n.6651-3C>G
XM_024450537.1:c.6651-3C>G	XP_024306305.1:n.6651-3C>G
NM_006445.4:c.6651-3C>G MANE Select	NP_006436.3:n.6651-3C>G