Canonical Allele Identifier: CA980683857

Gene: PRPF8

Linked Data

• dbSNP Id: rs1910989862
• gnomAD v3: 17-1650786-G-C
• gnomAD v4: 17-1650786-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1650786G>C , CM000679.2:g.1650786G>C	GRCh38
NC_000017.10:g.1554080G>C , CM000679.1:g.1554080G>C	GRCh37
NC_000017.9:g.1500830G>C	NCBI36
NG_009118.1:g.39097C>G
NG_033061.1:g.4313C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000573725.2:c.*16C>G	ENSP00000460849.2:n.*16C>G
ENST00000703537.1:c.2772C>G
ENST00000703538.1:c.*6747C>G	ENSP00000515361.1:n.*6747C>G
ENST00000703539.1:n.3338C>G
ENST00000703540.1:c.*16C>G	ENSP00000515362.1:n.*16C>G
ENST00000304992.11:c.*16C>G MANE Select	ENSP00000304350.6:n.*16C>G
ENST00000304992.10:c.*16C>G	ENSP00000304350.6:n.*16C>G
ENST00000571958.1:c.223C>G
ENST00000572621.5:c.*16C>G	ENSP00000460348.1:n.*16C>G
NM_006445.3:c.*16C>G	NP_006436.3:n.*16C>G
XM_024450537.1:c.*16C>G	XP_024306305.1:n.*16C>G
NM_006445.4:c.*16C>G MANE Select	NP_006436.3:n.*16C>G