Canonical Allele Identifier: CA2635248139

Gene: PRPF8

Linked Data

• gnomAD v4: 17-1650664-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1650664C>T , CM000679.2:g.1650664C>T	GRCh38
NC_000017.10:g.1553958C>T , CM000679.1:g.1553958C>T	GRCh37
NC_000017.9:g.1500708C>T	NCBI36
NG_009118.1:g.39219G>A
NG_033061.1:g.4435G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000573725.2:c.*138G>A	ENSP00000460849.2:n.*138G>A
ENST00000703537.1:c.2894G>A
ENST00000703538.1:c.*6869G>A	ENSP00000515361.1:n.*6869G>A
ENST00000703539.1:n.3460G>A
ENST00000703540.1:c.*138G>A	ENSP00000515362.1:n.*138G>A
ENST00000304992.11:c.*138G>A MANE Select	ENSP00000304350.6:n.*138G>A
ENST00000304992.10:c.*138G>A	ENSP00000304350.6:n.*138G>A
ENST00000571958.1:c.345G>A
ENST00000572621.5:c.*138G>A	ENSP00000460348.1:n.*138G>A
NM_006445.3:c.*138G>A	NP_006436.3:n.*138G>A
XM_024450537.1:c.*138G>A	XP_024306305.1:n.*138G>A
NM_006445.4:c.*138G>A MANE Select	NP_006436.3:n.*138G>A