Canonical Allele Identifier: CA2647799611

Gene: PRPF3

Linked Data

• gnomAD v4: 1-150346638-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150346638A>G , CM000663.2:g.150346638A>G	GRCh38
NC_000001.10:g.150319114A>G , CM000663.1:g.150319114A>G	GRCh37
NC_000001.9:g.148585738A>G	NCBI36
NG_008245.1:g.30187A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324862.7:c.1843+147A>G MANE Select	ENSP00000315379.6:n.1843+147A>G
ENST00000324862.6:c.1843+147A>G	ENSP00000315379.6:n.1843+147A>G
ENST00000467329.5:n.2170+147A>G
ENST00000476970.1:n.952+147A>G
NM_004698.2:c.1843+147A>G	NP_004689.1:n.1843+147A>G
XM_011510128.1:c.1853+137A>G	XP_011508430.1:n.1853+137A>G
XM_011510129.1:c.1438+147A>G	XP_011508431.1:n.1438+147A>G
XM_011510130.1:c.1411+147A>G	XP_011508432.1:n.1411+147A>G
XR_241103.1:n.1826+147A>G
XR_921997.1:n.1836+137A>G
XR_921998.1:n.1940+147A>G
NM_001350529.1:c.1438+147A>G	NP_001337458.1:n.1438+147A>G
NM_004698.3:c.1843+147A>G	NP_004689.1:n.1843+147A>G
NR_146766.1:n.2074+147A>G
NR_146767.1:n.2170+147A>G
NR_146768.1:n.2026+137A>G
NR_146769.1:n.2079+137A>G
XM_011510130.3:c.1411+147A>G	XP_011508432.1:n.1411+147A>G
XM_017002790.1:c.1411+147A>G	XP_016858279.1:n.1411+147A>G
XR_001737536.2:n.1876+147A>G
XR_001737537.2:n.1990+147A>G
XR_001737540.2:n.2747+147A>G
XR_001737541.2:n.1770+147A>G
XR_002958009.1:n.2500+147A>G
XR_002958010.1:n.3746+137A>G
XR_002958012.1:n.1942+137A>G
XR_241103.3:n.1818+147A>G
XR_921997.3:n.1828+137A>G
XR_921998.3:n.1932+147A>G
NM_004698.4:c.1843+147A>G MANE Select	NP_004689.1:n.1843+147A>G