Canonical Allele Identifier: CA397564203

Gene: PRPF8

Linked Data

• MyVariant Identifiers: chr17:g.1554600T>C (hg19) ; chr17:g.1651306T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1651306T>C , CM000679.2:g.1651306T>C	GRCh38
NC_000017.10:g.1554600T>C , CM000679.1:g.1554600T>C	GRCh37
NC_000017.9:g.1501350T>C	NCBI36
NG_009118.1:g.38577A>G
NG_033061.1:g.3793A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000573725.2:c.6475A>G	ENSP00000460849.2:p.Thr2159Ala
ENST00000703537.1:c.2403A>G
ENST00000703538.1:c.*6378A>G	ENSP00000515361.1:n.*6378A>G
ENST00000703539.1:n.2969A>G
ENST00000703540.1:c.6508A>G	ENSP00000515362.1:p.Thr2170Ala
ENST00000703541.1:c.6520A>G	ENSP00000515363.1:p.Thr2174Ala
ENST00000304992.11:c.6655A>G MANE Select	ENSP00000304350.6:p.Thr2219Ala
ENST00000304992.10:c.6655A>G	ENSP00000304350.6:p.Thr2219Ala
ENST00000572621.5:c.6655A>G	ENSP00000460348.1:p.Thr2219Ala
ENST00000572723.1:n.644A>G
NM_006445.3:c.6655A>G	NP_006436.3:p.Thr2219Ala
XM_024450537.1:c.6655A>G	XP_024306305.1:p.Thr2219Ala
NM_006445.4:c.6655A>G MANE Select	NP_006436.3:p.Thr2219Ala