Canonical Allele Identifier: CA342285606

Gene: PRPF3

Linked Data

• MyVariant Identifiers: chr1:g.150318944A>G (hg19) ; chr1:g.150346468A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150346468A>G , CM000663.2:g.150346468A>G	GRCh38
NC_000001.10:g.150318944A>G , CM000663.1:g.150318944A>G	GRCh37
NC_000001.9:g.148585568A>G	NCBI36
NG_008245.1:g.30017A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324862.7:c.1820A>G MANE Select	ENSP00000315379.6:p.Gln607Arg
ENST00000324862.6:c.1820A>G	ENSP00000315379.6:p.Gln607Arg
ENST00000467329.5:n.2147A>G
ENST00000476970.1:n.929A>G
NM_004698.2:c.1820A>G	NP_004689.1:p.Gln607Arg
XM_011510128.1:c.1820A>G	XP_011508430.1:p.Gln607Arg
XM_011510129.1:c.1415A>G	XP_011508431.1:p.Gln472Arg
XM_011510130.1:c.1388A>G	XP_011508432.1:p.Gln463Arg
XR_241103.1:n.1803A>G
XR_921997.1:n.1803A>G
XR_921998.1:n.1917A>G
NM_001350529.1:c.1415A>G	NP_001337458.1:p.Gln472Arg
NM_004698.3:c.1820A>G	NP_004689.1:p.Gln607Arg
NR_146766.1:n.2051A>G
NR_146767.1:n.2147A>G
NR_146768.1:n.1993A>G
NR_146769.1:n.2046A>G
XM_011510130.3:c.1388A>G	XP_011508432.1:p.Gln463Arg
XM_017002790.1:c.1388A>G	XP_016858279.1:p.Gln463Arg
XR_001737536.2:n.1853A>G
XR_001737537.2:n.1967A>G
XR_001737540.2:n.2724A>G
XR_001737541.2:n.1747A>G
XR_002958009.1:n.2477A>G
XR_002958010.1:n.3713A>G
XR_002958012.1:n.1909A>G
XR_241103.3:n.1795A>G
XR_921997.3:n.1795A>G
XR_921998.3:n.1909A>G
NM_004698.4:c.1820A>G MANE Select	NP_004689.1:p.Gln607Arg