Canonical Allele Identifier: CA397564146

Gene: PRPF8

Linked Data

• dbSNP Id: rs1283212744
• gnomAD v3: 17-1651278-T-G
• gnomAD v4: 17-1651278-T-G
• MyVariant Identifiers: chr17:g.1554572T>G (hg19) ; chr17:g.1651278T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1651278T>G , CM000679.2:g.1651278T>G	GRCh38
NC_000017.10:g.1554572T>G , CM000679.1:g.1554572T>G	GRCh37
NC_000017.9:g.1501322T>G	NCBI36
NG_009118.1:g.38605A>C
NG_033061.1:g.3821A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000573725.2:c.6503A>C	ENSP00000460849.2:p.Tyr2168Ser
ENST00000703537.1:c.2431A>C
ENST00000703538.1:c.*6406A>C	ENSP00000515361.1:n.*6406A>C
ENST00000703539.1:n.2997A>C
ENST00000703540.1:c.6536A>C	ENSP00000515362.1:p.Tyr2179Ser
ENST00000703541.1:c.6548A>C	ENSP00000515363.1:p.Tyr2183Ser
ENST00000304992.11:c.6683A>C MANE Select	ENSP00000304350.6:p.Tyr2228Ser
ENST00000304992.10:c.6683A>C	ENSP00000304350.6:p.Tyr2228Ser
ENST00000572621.5:c.6683A>C	ENSP00000460348.1:p.Tyr2228Ser
ENST00000572723.1:n.672A>C
NM_006445.3:c.6683A>C	NP_006436.3:p.Tyr2228Ser
XM_024450537.1:c.6683A>C	XP_024306305.1:p.Tyr2228Ser
NM_006445.4:c.6683A>C MANE Select	NP_006436.3:p.Tyr2228Ser