Canonical Allele Identifier: CA397563059

Gene: PRPF8

Linked Data

• MyVariant Identifiers: chr17:g.1582940T>A (hg19) ; chr17:g.1679646T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1679646T>A , CM000679.2:g.1679646T>A	GRCh38
NC_000017.10:g.1582940T>A , CM000679.1:g.1582940T>A	GRCh37
NC_000017.9:g.1529690T>A	NCBI36
NG_009118.1:g.10237A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000573725.2:c.1252A>T	ENSP00000460849.2:p.Thr418Ser
ENST00000703538.1:c.*975A>T	ENSP00000515361.1:n.*975A>T
ENST00000703540.1:c.1252A>T	ENSP00000515362.1:p.Thr418Ser
ENST00000703541.1:c.1252A>T	ENSP00000515363.1:p.Thr418Ser
ENST00000703542.1:n.1052A>T
ENST00000304992.11:c.1252A>T MANE Select	ENSP00000304350.6:p.Thr418Ser
ENST00000304992.10:c.1252A>T	ENSP00000304350.6:p.Thr418Ser
ENST00000572621.5:c.1252A>T	ENSP00000460348.1:p.Thr418Ser
ENST00000577001.1:c.1087A>T	ENSP00000458151.1:p.Thr363Ser
NM_006445.3:c.1252A>T	NP_006436.3:p.Thr418Ser
XM_024450537.1:c.1252A>T	XP_024306305.1:p.Thr418Ser
NM_006445.4:c.1252A>T MANE Select	NP_006436.3:p.Thr418Ser