Canonical Allele Identifier: CA497291452

Gene: PRPF8

Linked Data

• MyVariant Identifiers: chr17:g.1554129A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1650835A>C , CM000679.2:g.1650835A>C	GRCh38
NC_000017.10:g.1554129A>C , CM000679.1:g.1554129A>C	GRCh37
NC_000017.9:g.1500879A>C	NCBI36
NG_009118.1:g.39048T>G
NG_033061.1:g.4264T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000573725.2:c.6795T>G	ENSP00000460849.2:p.Val2265=
ENST00000703537.1:c.2723T>G
ENST00000703538.1:c.*6698T>G	ENSP00000515361.1:n.*6698T>G
ENST00000703539.1:n.3289T>G
ENST00000703540.1:c.6828T>G	ENSP00000515362.1:p.Val2276=
ENST00000703541.1:c.6840T>G	ENSP00000515363.1:p.Val2280=
ENST00000304992.11:c.6975T>G MANE Select	ENSP00000304350.6:p.Val2325=
ENST00000304992.10:c.6975T>G	ENSP00000304350.6:p.Val2325=
ENST00000571958.1:c.174T>G
ENST00000572621.5:c.6975T>G	ENSP00000460348.1:p.Val2325=
NM_006445.3:c.6975T>G	NP_006436.3:p.Val2325=
XM_024450537.1:c.6975T>G	XP_024306305.1:p.Val2325=
NM_006445.4:c.6975T>G MANE Select	NP_006436.3:p.Val2325=