Canonical Allele Identifier: CA397561878

Gene: PRPF8

Linked Data

• MyVariant Identifiers: chr17:g.1554148A>G (hg19) ; chr17:g.1650854A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1650854A>G , CM000679.2:g.1650854A>G	GRCh38
NC_000017.10:g.1554148A>G , CM000679.1:g.1554148A>G	GRCh37
NC_000017.9:g.1500898A>G	NCBI36
NG_009118.1:g.39029T>C
NG_033061.1:g.4245T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000573725.2:c.6776T>C	ENSP00000460849.2:p.Leu2259Pro
ENST00000703537.1:c.2704T>C
ENST00000703538.1:c.*6679T>C	ENSP00000515361.1:n.*6679T>C
ENST00000703539.1:n.3270T>C
ENST00000703540.1:c.6809T>C	ENSP00000515362.1:p.Leu2270Pro
ENST00000703541.1:c.6821T>C	ENSP00000515363.1:p.Leu2274Pro
ENST00000304992.11:c.6956T>C MANE Select	ENSP00000304350.6:p.Leu2319Pro
ENST00000304992.10:c.6956T>C	ENSP00000304350.6:p.Leu2319Pro
ENST00000571958.1:c.163-8T>C
ENST00000572621.5:c.6956T>C	ENSP00000460348.1:p.Leu2319Pro
ENST00000572723.1:n.945T>C
NM_006445.3:c.6956T>C	NP_006436.3:p.Leu2319Pro
XM_024450537.1:c.6956T>C	XP_024306305.1:p.Leu2319Pro
NM_006445.4:c.6956T>C MANE Select	NP_006436.3:p.Leu2319Pro