Canonical Allele Identifier: CA8271091

Gene: PRPF8

Linked Data

• dbSNP Id: rs375792310
• ExAC: 17:1554430 G / A
• gnomAD v2: 17-1554430-G-A
• gnomAD v3: 17-1651136-G-A
• gnomAD v4: 17-1651136-G-A
• MyVariant Identifiers: chr17:g.1554430G>A (hg19) ; chr17:g.1651136G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1651136G>A , CM000679.2:g.1651136G>A	GRCh38
NC_000017.10:g.1554430G>A , CM000679.1:g.1554430G>A	GRCh37
NC_000017.9:g.1501180G>A	NCBI36
NG_009118.1:g.38747C>T
NG_033061.1:g.3963C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000573725.2:c.6645C>T	ENSP00000460849.2:p.Ala2215=
ENST00000703537.1:c.2573C>T
ENST00000703538.1:c.*6548C>T	ENSP00000515361.1:n.*6548C>T
ENST00000703539.1:n.3139C>T
ENST00000703540.1:c.6678C>T	ENSP00000515362.1:p.Ala2226=
ENST00000703541.1:c.6690C>T	ENSP00000515363.1:p.Ala2230=
ENST00000304992.11:c.6825C>T MANE Select	ENSP00000304350.6:p.Ala2275=
ENST00000304992.10:c.6825C>T	ENSP00000304350.6:p.Ala2275=
ENST00000571958.1:c.134C>T
ENST00000572621.5:c.6825C>T	ENSP00000460348.1:p.Ala2275=
ENST00000572723.1:n.814C>T
NM_006445.3:c.6825C>T	NP_006436.3:p.Ala2275=
XM_024450537.1:c.6825C>T	XP_024306305.1:p.Ala2275=
NM_006445.4:c.6825C>T MANE Select	NP_006436.3:p.Ala2275=