Canonical Allele Identifier: CA397562096

Gene: PRPF8

Linked Data

• COSMIC: COSM975792
• MyVariant Identifiers: chr17:g.1554186G>T (hg19) ; chr17:g.1650892G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1650892G>T , CM000679.2:g.1650892G>T	GRCh38
NC_000017.10:g.1554186G>T , CM000679.1:g.1554186G>T	GRCh37
NC_000017.9:g.1500936G>T	NCBI36
NG_009118.1:g.38991C>A
NG_033061.1:g.4207C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000573725.2:c.6738C>A	ENSP00000460849.2:p.His2246Gln
ENST00000703537.1:c.2666C>A
ENST00000703538.1:c.*6641C>A	ENSP00000515361.1:n.*6641C>A
ENST00000703539.1:n.3232C>A
ENST00000703540.1:c.6771C>A	ENSP00000515362.1:p.His2257Gln
ENST00000703541.1:c.6783C>A	ENSP00000515363.1:p.His2261Gln
ENST00000304992.11:c.6918C>A MANE Select	ENSP00000304350.6:p.His2306Gln
ENST00000304992.10:c.6918C>A	ENSP00000304350.6:p.His2306Gln
ENST00000571958.1:c.163-46C>A
ENST00000572621.5:c.6918C>A	ENSP00000460348.1:p.His2306Gln
ENST00000572723.1:n.907C>A
NM_006445.3:c.6918C>A	NP_006436.3:p.His2306Gln
XM_024450537.1:c.6918C>A	XP_024306305.1:p.His2306Gln
NM_006445.4:c.6918C>A MANE Select	NP_006436.3:p.His2306Gln