Canonical Allele Identifier: CA497388910

Gene: PRPF8

Linked Data

• gnomAD v4: 17-1651217-G-C
• MyVariant Identifiers: chr17:g.1554511G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1651217G>C , CM000679.2:g.1651217G>C	GRCh38
NC_000017.10:g.1554511G>C , CM000679.1:g.1554511G>C	GRCh37
NC_000017.9:g.1501261G>C	NCBI36
NG_009118.1:g.38666C>G
NG_033061.1:g.3882C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000573725.2:c.6564C>G	ENSP00000460849.2:p.Pro2188=
ENST00000703537.1:c.2492C>G
ENST00000703538.1:c.*6467C>G	ENSP00000515361.1:n.*6467C>G
ENST00000703539.1:n.3058C>G
ENST00000703540.1:c.6597C>G	ENSP00000515362.1:p.Pro2199=
ENST00000703541.1:c.6609C>G	ENSP00000515363.1:p.Pro2203=
ENST00000304992.11:c.6744C>G MANE Select	ENSP00000304350.6:p.Pro2248=
ENST00000304992.10:c.6744C>G	ENSP00000304350.6:p.Pro2248=
ENST00000571958.1:c.53C>G
ENST00000572621.5:c.6744C>G	ENSP00000460348.1:p.Pro2248=
ENST00000572723.1:n.733C>G
NM_006445.3:c.6744C>G	NP_006436.3:p.Pro2248=
XM_024450537.1:c.6744C>G	XP_024306305.1:p.Pro2248=
NM_006445.4:c.6744C>G MANE Select	NP_006436.3:p.Pro2248=