Canonical Allele Identifier: CA526033811

Gene: PRPF3

Linked Data

• dbSNP Id: rs1327473120
• gnomAD v2: 1-150319200-TC-T
• gnomAD v3: 1-150346724-TC-T
• gnomAD v4: 1-150346724-TC-T
• MyVariant Identifiers: chr1:g.150319201del (hg19) ; chr1:g.150346725del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150346725del , CM000663.2:g.150346725del	GRCh38
NC_000001.10:g.150319201del , CM000663.1:g.150319201del	GRCh37
NC_000001.9:g.148585825del	NCBI36
NG_008245.1:g.30274del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324862.7:c.1843+234del MANE Select	ENSP00000315379.6:n.1843+234del
ENST00000324862.6:c.1843+234del	ENSP00000315379.6:n.1843+234del
ENST00000467329.5:n.2170+234del
ENST00000476970.1:n.952+234del
NM_004698.2:c.1843+234del	NP_004689.1:n.1843+234del
XM_011510128.1:c.1853+224del	XP_011508430.1:n.1853+224del
XM_011510129.1:c.1438+234del	XP_011508431.1:n.1438+234del
XM_011510130.1:c.1411+234del	XP_011508432.1:n.1411+234del
XR_241103.1:n.1826+234del
XR_921997.1:n.1836+224del
XR_921998.1:n.1940+234del
NM_001350529.1:c.1438+234del	NP_001337458.1:n.1438+234del
NM_004698.3:c.1843+234del	NP_004689.1:n.1843+234del
NR_146766.1:n.2074+234del
NR_146767.1:n.2170+234del
NR_146768.1:n.2026+224del
NR_146769.1:n.2079+224del
XM_011510130.3:c.1411+234del	XP_011508432.1:n.1411+234del
XM_017002790.1:c.1411+234del	XP_016858279.1:n.1411+234del
XR_001737536.2:n.1876+234del
XR_001737537.2:n.1990+234del
XR_001737540.2:n.2747+234del
XR_001737541.2:n.1770+234del
XR_002958009.1:n.2500+234del
XR_002958010.1:n.3746+224del
XR_002958012.1:n.1942+224del
XR_241103.3:n.1818+234del
XR_921997.3:n.1828+224del
XR_921998.3:n.1932+234del
NM_004698.4:c.1843+234del MANE Select	NP_004689.1:n.1843+234del