Canonical Allele Identifier: CA397561714

Gene: PRPF8

Linked Data

• MyVariant Identifiers: chr17:g.1554109T>G (hg19) ; chr17:g.1650815T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1650815T>G , CM000679.2:g.1650815T>G	GRCh38
NC_000017.10:g.1554109T>G , CM000679.1:g.1554109T>G	GRCh37
NC_000017.9:g.1500859T>G	NCBI36
NG_009118.1:g.39068A>C
NG_033061.1:g.4284A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000573725.2:c.6815A>C	ENSP00000460849.2:p.Asp2272Ala
ENST00000703537.1:c.2743A>C
ENST00000703538.1:c.*6718A>C	ENSP00000515361.1:n.*6718A>C
ENST00000703539.1:n.3309A>C
ENST00000703540.1:c.6848A>C	ENSP00000515362.1:p.Asp2283Ala
ENST00000703541.1:c.6860A>C	ENSP00000515363.1:p.Asp2287Ala
ENST00000304992.11:c.6995A>C MANE Select	ENSP00000304350.6:p.Asp2332Ala
ENST00000304992.10:c.6995A>C	ENSP00000304350.6:p.Asp2332Ala
ENST00000571958.1:c.194A>C
ENST00000572621.5:c.6995A>C	ENSP00000460348.1:p.Asp2332Ala
NM_006445.3:c.6995A>C	NP_006436.3:p.Asp2332Ala
XM_024450537.1:c.6995A>C	XP_024306305.1:p.Asp2332Ala
NM_006445.4:c.6995A>C MANE Select	NP_006436.3:p.Asp2332Ala