Canonical Allele Identifier: CA526033809

Gene: PRPF3

Linked Data

• dbSNP Id: rs1553873047
• gnomAD v2: 1-150319188-A-T
• MyVariant Identifiers: chr1:g.150319188A>T (hg19) ; chr1:g.150346712A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150346712A>T , CM000663.2:g.150346712A>T	GRCh38
NC_000001.10:g.150319188A>T , CM000663.1:g.150319188A>T	GRCh37
NC_000001.9:g.148585812A>T	NCBI36
NG_008245.1:g.30261A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324862.7:c.1843+221A>T MANE Select	ENSP00000315379.6:n.1843+221A>T
ENST00000324862.6:c.1843+221A>T	ENSP00000315379.6:n.1843+221A>T
ENST00000467329.5:n.2170+221A>T
ENST00000476970.1:n.952+221A>T
NM_004698.2:c.1843+221A>T	NP_004689.1:n.1843+221A>T
XM_011510128.1:c.1853+211A>T	XP_011508430.1:n.1853+211A>T
XM_011510129.1:c.1438+221A>T	XP_011508431.1:n.1438+221A>T
XM_011510130.1:c.1411+221A>T	XP_011508432.1:n.1411+221A>T
XR_241103.1:n.1826+221A>T
XR_921997.1:n.1836+211A>T
XR_921998.1:n.1940+221A>T
NM_001350529.1:c.1438+221A>T	NP_001337458.1:n.1438+221A>T
NM_004698.3:c.1843+221A>T	NP_004689.1:n.1843+221A>T
NR_146766.1:n.2074+221A>T
NR_146767.1:n.2170+221A>T
NR_146768.1:n.2026+211A>T
NR_146769.1:n.2079+211A>T
XM_011510130.3:c.1411+221A>T	XP_011508432.1:n.1411+221A>T
XM_017002790.1:c.1411+221A>T	XP_016858279.1:n.1411+221A>T
XR_001737536.2:n.1876+221A>T
XR_001737537.2:n.1990+221A>T
XR_001737540.2:n.2747+221A>T
XR_001737541.2:n.1770+221A>T
XR_002958009.1:n.2500+221A>T
XR_002958010.1:n.3746+211A>T
XR_002958012.1:n.1942+211A>T
XR_241103.3:n.1818+221A>T
XR_921997.3:n.1828+211A>T
XR_921998.3:n.1932+221A>T
NM_004698.4:c.1843+221A>T MANE Select	NP_004689.1:n.1843+221A>T