Canonical Allele Identifier: CA397561802

Gene: PRPF8

Linked Data

• MyVariant Identifiers: chr17:g.1554132C>G (hg19) ; chr17:g.1650838C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1650838C>G , CM000679.2:g.1650838C>G	GRCh38
NC_000017.10:g.1554132C>G , CM000679.1:g.1554132C>G	GRCh37
NC_000017.9:g.1500882C>G	NCBI36
NG_009118.1:g.39045G>C
NG_033061.1:g.4261G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000573725.2:c.6792G>C	ENSP00000460849.2:p.Glu2264Asp
ENST00000703537.1:c.2720G>C
ENST00000703538.1:c.*6695G>C	ENSP00000515361.1:n.*6695G>C
ENST00000703539.1:n.3286G>C
ENST00000703540.1:c.6825G>C	ENSP00000515362.1:p.Glu2275Asp
ENST00000703541.1:c.6837G>C	ENSP00000515363.1:p.Glu2279Asp
ENST00000304992.11:c.6972G>C MANE Select	ENSP00000304350.6:p.Glu2324Asp
ENST00000304992.10:c.6972G>C	ENSP00000304350.6:p.Glu2324Asp
ENST00000571958.1:c.171G>C
ENST00000572621.5:c.6972G>C	ENSP00000460348.1:p.Glu2324Asp
NM_006445.3:c.6972G>C	NP_006436.3:p.Glu2324Asp
XM_024450537.1:c.6972G>C	XP_024306305.1:p.Glu2324Asp
NM_006445.4:c.6972G>C MANE Select	NP_006436.3:p.Glu2324Asp