Canonical Allele Identifier: CA342285316

Gene: PRPF3

Linked Data

• MyVariant Identifiers: chr1:g.150318922C>G (hg19) ; chr1:g.150346446C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150346446C>G , CM000663.2:g.150346446C>G	GRCh38
NC_000001.10:g.150318922C>G , CM000663.1:g.150318922C>G	GRCh37
NC_000001.9:g.148585546C>G	NCBI36
NG_008245.1:g.29995C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324862.7:c.1798C>G MANE Select	ENSP00000315379.6:p.His600Asp
ENST00000324862.6:c.1798C>G	ENSP00000315379.6:p.His600Asp
ENST00000467329.5:n.2125C>G
ENST00000476970.1:n.907C>G
NM_004698.2:c.1798C>G	NP_004689.1:p.His600Asp
XM_011510128.1:c.1798C>G	XP_011508430.1:p.His600Asp
XM_011510129.1:c.1393C>G	XP_011508431.1:p.His465Asp
XM_011510130.1:c.1366C>G	XP_011508432.1:p.His456Asp
XR_241103.1:n.1781C>G
XR_921997.1:n.1781C>G
XR_921998.1:n.1895C>G
NM_001350529.1:c.1393C>G	NP_001337458.1:p.His465Asp
NM_004698.3:c.1798C>G	NP_004689.1:p.His600Asp
NR_146766.1:n.2029C>G
NR_146767.1:n.2125C>G
NR_146768.1:n.1971C>G
NR_146769.1:n.2024C>G
XM_011510130.3:c.1366C>G	XP_011508432.1:p.His456Asp
XM_017002790.1:c.1366C>G	XP_016858279.1:p.His456Asp
XR_001737536.2:n.1831C>G
XR_001737537.2:n.1945C>G
XR_001737540.2:n.2702C>G
XR_001737541.2:n.1725C>G
XR_002958009.1:n.2455C>G
XR_002958010.1:n.3691C>G
XR_002958012.1:n.1887C>G
XR_241103.3:n.1773C>G
XR_921997.3:n.1773C>G
XR_921998.3:n.1887C>G
NM_004698.4:c.1798C>G MANE Select	NP_004689.1:p.His600Asp