Canonical Allele Identifier: CA397563707

Gene: PRPF8

Linked Data

• MyVariant Identifiers: chr17:g.1554441T>C (hg19) ; chr17:g.1651147T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1651147T>C , CM000679.2:g.1651147T>C	GRCh38
NC_000017.10:g.1554441T>C , CM000679.1:g.1554441T>C	GRCh37
NC_000017.9:g.1501191T>C	NCBI36
NG_009118.1:g.38736A>G
NG_033061.1:g.3952A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000573725.2:c.6634A>G	ENSP00000460849.2:p.Met2212Val
ENST00000703537.1:c.2562A>G
ENST00000703538.1:c.*6537A>G	ENSP00000515361.1:n.*6537A>G
ENST00000703539.1:n.3128A>G
ENST00000703540.1:c.6667A>G	ENSP00000515362.1:p.Met2223Val
ENST00000703541.1:c.6679A>G	ENSP00000515363.1:p.Met2227Val
ENST00000304992.11:c.6814A>G MANE Select	ENSP00000304350.6:p.Met2272Val
ENST00000304992.10:c.6814A>G	ENSP00000304350.6:p.Met2272Val
ENST00000571958.1:c.123A>G
ENST00000572621.5:c.6814A>G	ENSP00000460348.1:p.Met2272Val
ENST00000572723.1:n.803A>G
NM_006445.3:c.6814A>G	NP_006436.3:p.Met2272Val
XM_024450537.1:c.6814A>G	XP_024306305.1:p.Met2272Val
NM_006445.4:c.6814A>G MANE Select	NP_006436.3:p.Met2272Val