Canonical Allele Identifier: CA374554781

Gene: PRPF4

Linked Data

• MyVariant Identifiers: chr9:g.116050492C>G (hg19) ; chr9:g.113288212C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113288212C>G , CM000671.2:g.113288212C>G	GRCh38
NC_000009.11:g.116050492C>G , CM000671.1:g.116050492C>G	GRCh37
NC_000009.10:g.115090313C>G	NCBI36
NG_034225.1:g.17579C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374198.5:c.970C>G MANE Select	ENSP00000363313.4:p.Arg324Gly
ENST00000374199.9:c.973C>G	ENSP00000363315.4:p.Arg325Gly
ENST00000374198.4:c.973C>G	ENSP00000363313.3:p.Arg325Gly
ENST00000374199.8:c.970C>G	ENSP00000363315.3:p.Arg324Gly
NM_001244926.1:c.970C>G	NP_001231855.1:p.Arg324Gly
NM_004697.4:c.973C>G	NP_004688.2:p.Arg325Gly
XM_005252300.2:c.244C>G	XP_005252357.1:p.Arg82Gly
XM_011519181.1:c.973C>G	XP_011517483.1:p.Arg325Gly
NM_001322266.1:c.244C>G	NP_001309195.1:p.Arg82Gly
NM_001322267.1:c.244C>G	NP_001309196.1:p.Arg82Gly
NR_136265.1:n.1083C>G
NR_136266.1:n.1080C>G
NM_001244926.2:c.970C>G MANE Select	NP_001231855.1:p.Arg324Gly
NM_001322266.2:c.244C>G	NP_001309195.1:p.Arg82Gly
NM_001322267.2:c.244C>G	NP_001309196.1:p.Arg82Gly
NM_004697.5:c.973C>G	NP_004688.2:p.Arg325Gly
NR_136265.2:n.1059C>G
NR_136266.2:n.1056C>G