Canonical Allele Identifier: CA397562404

Gene: PRPF8

Linked Data

• MyVariant Identifiers: chr17:g.1554224A>T (hg19) ; chr17:g.1650930A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1650930A>T , CM000679.2:g.1650930A>T	GRCh38
NC_000017.10:g.1554224A>T , CM000679.1:g.1554224A>T	GRCh37
NC_000017.9:g.1500974A>T	NCBI36
NG_009118.1:g.38953T>A
NG_033061.1:g.4169T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000573725.2:c.6700T>A	ENSP00000460849.2:p.Tyr2234Asn
ENST00000703537.1:c.2628T>A
ENST00000703538.1:c.*6603T>A	ENSP00000515361.1:n.*6603T>A
ENST00000703539.1:n.3194T>A
ENST00000703540.1:c.6733T>A	ENSP00000515362.1:p.Tyr2245Asn
ENST00000703541.1:c.6745T>A	ENSP00000515363.1:p.Tyr2249Asn
ENST00000304992.11:c.6880T>A MANE Select	ENSP00000304350.6:p.Tyr2294Asn
ENST00000304992.10:c.6880T>A	ENSP00000304350.6:p.Tyr2294Asn
ENST00000571958.1:c.163-84T>A
ENST00000572621.5:c.6880T>A	ENSP00000460348.1:p.Tyr2294Asn
ENST00000572723.1:n.869T>A
NM_006445.3:c.6880T>A	NP_006436.3:p.Tyr2294Asn
XM_024450537.1:c.6880T>A	XP_024306305.1:p.Tyr2294Asn
NM_006445.4:c.6880T>A MANE Select	NP_006436.3:p.Tyr2294Asn