Canonical Allele Identifier: CA466759058

Gene: PRPF4

Linked Data

• MyVariant Identifiers: chr9:g.116050542C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113288262C>A , CM000671.2:g.113288262C>A	GRCh38
NC_000009.11:g.116050542C>A , CM000671.1:g.116050542C>A	GRCh37
NC_000009.10:g.115090363C>A	NCBI36
NG_034225.1:g.17629C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374198.5:c.1020C>A MANE Select	ENSP00000363313.4:p.Thr340=
ENST00000374199.9:c.1023C>A	ENSP00000363315.4:p.Thr341=
ENST00000374198.4:c.1023C>A	ENSP00000363313.3:p.Thr341=
ENST00000374199.8:c.1020C>A	ENSP00000363315.3:p.Thr340=
NM_001244926.1:c.1020C>A	NP_001231855.1:p.Thr340=
NM_004697.4:c.1023C>A	NP_004688.2:p.Thr341=
XM_005252300.2:c.294C>A	XP_005252357.1:p.Thr98=
XM_011519181.1:c.1023C>A	XP_011517483.1:p.Thr341=
NM_001322266.1:c.294C>A	NP_001309195.1:p.Thr98=
NM_001322267.1:c.294C>A	NP_001309196.1:p.Thr98=
NR_136265.1:n.1133C>A
NR_136266.1:n.1130C>A
NM_001244926.2:c.1020C>A MANE Select	NP_001231855.1:p.Thr340=
NM_001322266.2:c.294C>A	NP_001309195.1:p.Thr98=
NM_001322267.2:c.294C>A	NP_001309196.1:p.Thr98=
NM_004697.5:c.1023C>A	NP_004688.2:p.Thr341=
NR_136265.2:n.1109C>A
NR_136266.2:n.1106C>A