Canonical Allele Identifier: CA397561988

Gene: PRPF8

Linked Data

• MyVariant Identifiers: chr17:g.1554170A>G (hg19) ; chr17:g.1650876A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1650876A>G , CM000679.2:g.1650876A>G	GRCh38
NC_000017.10:g.1554170A>G , CM000679.1:g.1554170A>G	GRCh37
NC_000017.9:g.1500920A>G	NCBI36
NG_009118.1:g.39007T>C
NG_033061.1:g.4223T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000573725.2:c.6754T>C	ENSP00000460849.2:p.Ser2252Pro
ENST00000703537.1:c.2682T>C
ENST00000703538.1:c.*6657T>C	ENSP00000515361.1:n.*6657T>C
ENST00000703539.1:n.3248T>C
ENST00000703540.1:c.6787T>C	ENSP00000515362.1:p.Ser2263Pro
ENST00000703541.1:c.6799T>C	ENSP00000515363.1:p.Ser2267Pro
ENST00000304992.11:c.6934T>C MANE Select	ENSP00000304350.6:p.Ser2312Pro
ENST00000304992.10:c.6934T>C	ENSP00000304350.6:p.Ser2312Pro
ENST00000571958.1:c.163-30T>C
ENST00000572621.5:c.6934T>C	ENSP00000460348.1:p.Ser2312Pro
ENST00000572723.1:n.923T>C
NM_006445.3:c.6934T>C	NP_006436.3:p.Ser2312Pro
XM_024450537.1:c.6934T>C	XP_024306305.1:p.Ser2312Pro
NM_006445.4:c.6934T>C MANE Select	NP_006436.3:p.Ser2312Pro