Canonical Allele Identifier: CA286849410

Gene: PRPF8

Linked Data

• dbSNP Id: rs370155582
• gnomAD v2: 17-1554093-C-T
• gnomAD v3: 17-1650799-C-T
• gnomAD v4: 17-1650799-C-T
• MyVariant Identifiers: chr17:g.1554093C>T (hg19) ; chr17:g.1650799C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1650799C>T , CM000679.2:g.1650799C>T	GRCh38
NC_000017.10:g.1554093C>T , CM000679.1:g.1554093C>T	GRCh37
NC_000017.9:g.1500843C>T	NCBI36
NG_009118.1:g.39084G>A
NG_033061.1:g.4300G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000573725.2:c.*3G>A	ENSP00000460849.2:n.*3G>A
ENST00000703537.1:c.2759G>A
ENST00000703538.1:c.*6734G>A	ENSP00000515361.1:n.*6734G>A
ENST00000703539.1:n.3325G>A
ENST00000703540.1:c.*3G>A	ENSP00000515362.1:n.*3G>A
ENST00000304992.11:c.*3G>A MANE Select	ENSP00000304350.6:n.*3G>A
ENST00000304992.10:c.*3G>A	ENSP00000304350.6:n.*3G>A
ENST00000571958.1:c.210G>A
ENST00000572621.5:c.*3G>A	ENSP00000460348.1:n.*3G>A
NM_006445.3:c.*3G>A	NP_006436.3:n.*3G>A
XM_024450537.1:c.*3G>A	XP_024306305.1:n.*3G>A
NM_006445.4:c.*3G>A MANE Select	NP_006436.3:n.*3G>A