Canonical Allele Identifier: CA397564123

Gene: PRPF8

Linked Data

• MyVariant Identifiers: chr17:g.1554561G>A (hg19) ; chr17:g.1651267G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1651267G>A , CM000679.2:g.1651267G>A	GRCh38
NC_000017.10:g.1554561G>A , CM000679.1:g.1554561G>A	GRCh37
NC_000017.9:g.1501311G>A	NCBI36
NG_009118.1:g.38616C>T
NG_033061.1:g.3832C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000573725.2:c.6514C>T	ENSP00000460849.2:p.Pro2172Ser
ENST00000703537.1:c.2442C>T
ENST00000703538.1:c.*6417C>T	ENSP00000515361.1:n.*6417C>T
ENST00000703539.1:n.3008C>T
ENST00000703540.1:c.6547C>T	ENSP00000515362.1:p.Pro2183Ser
ENST00000703541.1:c.6559C>T	ENSP00000515363.1:p.Pro2187Ser
ENST00000304992.11:c.6694C>T MANE Select	ENSP00000304350.6:p.Pro2232Ser
ENST00000304992.10:c.6694C>T	ENSP00000304350.6:p.Pro2232Ser
ENST00000571958.1:c.3C>T
ENST00000572621.5:c.6694C>T	ENSP00000460348.1:p.Pro2232Ser
ENST00000572723.1:n.683C>T
NM_006445.3:c.6694C>T	NP_006436.3:p.Pro2232Ser
XM_024450537.1:c.6694C>T	XP_024306305.1:p.Pro2232Ser
NM_006445.4:c.6694C>T MANE Select	NP_006436.3:p.Pro2232Ser