Canonical Allele Identifier: CA497291505

Gene: PRPF8

Linked Data

• MyVariant Identifiers: chr17:g.1554147G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1650853G>T , CM000679.2:g.1650853G>T	GRCh38
NC_000017.10:g.1554147G>T , CM000679.1:g.1554147G>T	GRCh37
NC_000017.9:g.1500897G>T	NCBI36
NG_009118.1:g.39030C>A
NG_033061.1:g.4246C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000573725.2:c.6777C>A	ENSP00000460849.2:p.Leu2259=
ENST00000703537.1:c.2705C>A
ENST00000703538.1:c.*6680C>A	ENSP00000515361.1:n.*6680C>A
ENST00000703539.1:n.3271C>A
ENST00000703540.1:c.6810C>A	ENSP00000515362.1:p.Leu2270=
ENST00000703541.1:c.6822C>A	ENSP00000515363.1:p.Leu2274=
ENST00000304992.11:c.6957C>A MANE Select	ENSP00000304350.6:p.Leu2319=
ENST00000304992.10:c.6957C>A	ENSP00000304350.6:p.Leu2319=
ENST00000571958.1:c.163-7C>A
ENST00000572621.5:c.6957C>A	ENSP00000460348.1:p.Leu2319=
ENST00000572723.1:n.946C>A
NM_006445.3:c.6957C>A	NP_006436.3:p.Leu2319=
XM_024450537.1:c.6957C>A	XP_024306305.1:p.Leu2319=
NM_006445.4:c.6957C>A MANE Select	NP_006436.3:p.Leu2319=