Canonical Allele Identifier: CA497291829

Gene: PRPF8

Linked Data

• MyVariant Identifiers: chr17:g.1554225T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1650931T>C , CM000679.2:g.1650931T>C	GRCh38
NC_000017.10:g.1554225T>C , CM000679.1:g.1554225T>C	GRCh37
NC_000017.9:g.1500975T>C	NCBI36
NG_009118.1:g.38952A>G
NG_033061.1:g.4168A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000573725.2:c.6699A>G	ENSP00000460849.2:p.Lys2233=
ENST00000703537.1:c.2627A>G
ENST00000703538.1:c.*6602A>G	ENSP00000515361.1:n.*6602A>G
ENST00000703539.1:n.3193A>G
ENST00000703540.1:c.6732A>G	ENSP00000515362.1:p.Lys2244=
ENST00000703541.1:c.6744A>G	ENSP00000515363.1:p.Lys2248=
ENST00000304992.11:c.6879A>G MANE Select	ENSP00000304350.6:p.Lys2293=
ENST00000304992.10:c.6879A>G	ENSP00000304350.6:p.Lys2293=
ENST00000571958.1:c.163-85A>G
ENST00000572621.5:c.6879A>G	ENSP00000460348.1:p.Lys2293=
ENST00000572723.1:n.868A>G
NM_006445.3:c.6879A>G	NP_006436.3:p.Lys2293=
XM_024450537.1:c.6879A>G	XP_024306305.1:p.Lys2293=
NM_006445.4:c.6879A>G MANE Select	NP_006436.3:p.Lys2293=