Canonical Allele Identifier: CA397563999

Gene: PRPF8

Linked Data

• MyVariant Identifiers: chr17:g.1554524T>A (hg19) ; chr17:g.1651230T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1651230T>A , CM000679.2:g.1651230T>A	GRCh38
NC_000017.10:g.1554524T>A , CM000679.1:g.1554524T>A	GRCh37
NC_000017.9:g.1501274T>A	NCBI36
NG_009118.1:g.38653A>T
NG_033061.1:g.3869A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000573725.2:c.6551A>T	ENSP00000460849.2:p.Lys2184Met
ENST00000703537.1:c.2479A>T
ENST00000703538.1:c.*6454A>T	ENSP00000515361.1:n.*6454A>T
ENST00000703539.1:n.3045A>T
ENST00000703540.1:c.6584A>T	ENSP00000515362.1:p.Lys2195Met
ENST00000703541.1:c.6596A>T	ENSP00000515363.1:p.Lys2199Met
ENST00000304992.11:c.6731A>T MANE Select	ENSP00000304350.6:p.Lys2244Met
ENST00000304992.10:c.6731A>T	ENSP00000304350.6:p.Lys2244Met
ENST00000571958.1:c.40A>T
ENST00000572621.5:c.6731A>T	ENSP00000460348.1:p.Lys2244Met
ENST00000572723.1:n.720A>T
NM_006445.3:c.6731A>T	NP_006436.3:p.Lys2244Met
XM_024450537.1:c.6731A>T	XP_024306305.1:p.Lys2244Met
NM_006445.4:c.6731A>T MANE Select	NP_006436.3:p.Lys2244Met