Canonical Allele Identifier: CA374554827

Gene: PRPF4

Linked Data

• MyVariant Identifiers: chr9:g.116050514A>G (hg19) ; chr9:g.113288234A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113288234A>G , CM000671.2:g.113288234A>G	GRCh38
NC_000009.11:g.116050514A>G , CM000671.1:g.116050514A>G	GRCh37
NC_000009.10:g.115090335A>G	NCBI36
NG_034225.1:g.17601A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374198.5:c.992A>G MANE Select	ENSP00000363313.4:p.His331Arg
ENST00000374199.9:c.995A>G	ENSP00000363315.4:p.His332Arg
ENST00000374198.4:c.995A>G	ENSP00000363313.3:p.His332Arg
ENST00000374199.8:c.992A>G	ENSP00000363315.3:p.His331Arg
NM_001244926.1:c.992A>G	NP_001231855.1:p.His331Arg
NM_004697.4:c.995A>G	NP_004688.2:p.His332Arg
XM_005252300.2:c.266A>G	XP_005252357.1:p.His89Arg
XM_011519181.1:c.995A>G	XP_011517483.1:p.His332Arg
NM_001322266.1:c.266A>G	NP_001309195.1:p.His89Arg
NM_001322267.1:c.266A>G	NP_001309196.1:p.His89Arg
NR_136265.1:n.1105A>G
NR_136266.1:n.1102A>G
NM_001244926.2:c.992A>G MANE Select	NP_001231855.1:p.His331Arg
NM_001322266.2:c.266A>G	NP_001309195.1:p.His89Arg
NM_001322267.2:c.266A>G	NP_001309196.1:p.His89Arg
NM_004697.5:c.995A>G	NP_004688.2:p.His332Arg
NR_136265.2:n.1081A>G
NR_136266.2:n.1078A>G