Canonical Allele Identifier: CA497388916

Gene: PRPF8

Linked Data

• MyVariant Identifiers: chr17:g.1554529T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1651235T>C , CM000679.2:g.1651235T>C	GRCh38
NC_000017.10:g.1554529T>C , CM000679.1:g.1554529T>C	GRCh37
NC_000017.9:g.1501279T>C	NCBI36
NG_009118.1:g.38648A>G
NG_033061.1:g.3864A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000573725.2:c.6546A>G	ENSP00000460849.2:p.Thr2182=
ENST00000703537.1:c.2474A>G
ENST00000703538.1:c.*6449A>G	ENSP00000515361.1:n.*6449A>G
ENST00000703539.1:n.3040A>G
ENST00000703540.1:c.6579A>G	ENSP00000515362.1:p.Thr2193=
ENST00000703541.1:c.6591A>G	ENSP00000515363.1:p.Thr2197=
ENST00000304992.11:c.6726A>G MANE Select	ENSP00000304350.6:p.Thr2242=
ENST00000304992.10:c.6726A>G	ENSP00000304350.6:p.Thr2242=
ENST00000571958.1:c.35A>G
ENST00000572621.5:c.6726A>G	ENSP00000460348.1:p.Thr2242=
ENST00000572723.1:n.715A>G
NM_006445.3:c.6726A>G	NP_006436.3:p.Thr2242=
XM_024450537.1:c.6726A>G	XP_024306305.1:p.Thr2242=
NM_006445.4:c.6726A>G MANE Select	NP_006436.3:p.Thr2242=