Canonical Allele Identifier: CA374554886

Gene: PRPF4

Linked Data

• MyVariant Identifiers: chr9:g.116050544G>C (hg19) ; chr9:g.113288264G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113288264G>C , CM000671.2:g.113288264G>C	GRCh38
NC_000009.11:g.116050544G>C , CM000671.1:g.116050544G>C	GRCh37
NC_000009.10:g.115090365G>C	NCBI36
NG_034225.1:g.17631G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374198.5:c.1022G>C MANE Select	ENSP00000363313.4:p.Cys341Ser
ENST00000374199.9:c.1025G>C	ENSP00000363315.4:p.Cys342Ser
ENST00000374198.4:c.1025G>C	ENSP00000363313.3:p.Cys342Ser
ENST00000374199.8:c.1022G>C	ENSP00000363315.3:p.Cys341Ser
NM_001244926.1:c.1022G>C	NP_001231855.1:p.Cys341Ser
NM_004697.4:c.1025G>C	NP_004688.2:p.Cys342Ser
XM_005252300.2:c.296G>C	XP_005252357.1:p.Cys99Ser
XM_011519181.1:c.1025G>C	XP_011517483.1:p.Cys342Ser
NM_001322266.1:c.296G>C	NP_001309195.1:p.Cys99Ser
NM_001322267.1:c.296G>C	NP_001309196.1:p.Cys99Ser
NR_136265.1:n.1135G>C
NR_136266.1:n.1132G>C
NM_001244926.2:c.1022G>C MANE Select	NP_001231855.1:p.Cys341Ser
NM_001322266.2:c.296G>C	NP_001309195.1:p.Cys99Ser
NM_001322267.2:c.296G>C	NP_001309196.1:p.Cys99Ser
NM_004697.5:c.1025G>C	NP_004688.2:p.Cys342Ser
NR_136265.2:n.1111G>C
NR_136266.2:n.1108G>C