Canonical Allele Identifier: CA374554847

Gene: PRPF4

Linked Data

• MyVariant Identifiers: chr9:g.116050523G>C (hg19) ; chr9:g.113288243G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113288243G>C , CM000671.2:g.113288243G>C	GRCh38
NC_000009.11:g.116050523G>C , CM000671.1:g.116050523G>C	GRCh37
NC_000009.10:g.115090344G>C	NCBI36
NG_034225.1:g.17610G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374198.5:c.1001G>C MANE Select	ENSP00000363313.4:p.Gly334Ala
ENST00000374199.9:c.1004G>C	ENSP00000363315.4:p.Gly335Ala
ENST00000374198.4:c.1004G>C	ENSP00000363313.3:p.Gly335Ala
ENST00000374199.8:c.1001G>C	ENSP00000363315.3:p.Gly334Ala
NM_001244926.1:c.1001G>C	NP_001231855.1:p.Gly334Ala
NM_004697.4:c.1004G>C	NP_004688.2:p.Gly335Ala
XM_005252300.2:c.275G>C	XP_005252357.1:p.Gly92Ala
XM_011519181.1:c.1004G>C	XP_011517483.1:p.Gly335Ala
NM_001322266.1:c.275G>C	NP_001309195.1:p.Gly92Ala
NM_001322267.1:c.275G>C	NP_001309196.1:p.Gly92Ala
NR_136265.1:n.1114G>C
NR_136266.1:n.1111G>C
NM_001244926.2:c.1001G>C MANE Select	NP_001231855.1:p.Gly334Ala
NM_001322266.2:c.275G>C	NP_001309195.1:p.Gly92Ala
NM_001322267.2:c.275G>C	NP_001309196.1:p.Gly92Ala
NM_004697.5:c.1004G>C	NP_004688.2:p.Gly335Ala
NR_136265.2:n.1090G>C
NR_136266.2:n.1087G>C