Canonical Allele Identifier: CA397561655

Gene: PRPF8

Linked Data

• MyVariant Identifiers: chr17:g.1554100G>C (hg19) ; chr17:g.1650806G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1650806G>C , CM000679.2:g.1650806G>C	GRCh38
NC_000017.10:g.1554100G>C , CM000679.1:g.1554100G>C	GRCh37
NC_000017.9:g.1500850G>C	NCBI36
NG_009118.1:g.39077C>G
NG_033061.1:g.4293C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000573725.2:c.6824C>G	ENSP00000460849.2:p.Ala2275Gly
ENST00000703537.1:c.2752C>G
ENST00000703538.1:c.*6727C>G	ENSP00000515361.1:n.*6727C>G
ENST00000703539.1:n.3318C>G
ENST00000703540.1:c.6857C>G	ENSP00000515362.1:p.Ala2286Gly
ENST00000703541.1:c.6869C>G	ENSP00000515363.1:p.Ala2290Gly
ENST00000304992.11:c.7004C>G MANE Select	ENSP00000304350.6:p.Ala2335Gly
ENST00000304992.10:c.7004C>G	ENSP00000304350.6:p.Ala2335Gly
ENST00000571958.1:c.203C>G
ENST00000572621.5:c.7004C>G	ENSP00000460348.1:p.Ala2335Gly
NM_006445.3:c.7004C>G	NP_006436.3:p.Ala2335Gly
XM_024450537.1:c.7004C>G	XP_024306305.1:p.Ala2335Gly
NM_006445.4:c.7004C>G MANE Select	NP_006436.3:p.Ala2335Gly