Canonical Allele Identifier: CA342285126

Gene: PRPF3

Linked Data

• MyVariant Identifiers: chr1:g.150318903A>T (hg19) ; chr1:g.150346427A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150346427A>T , CM000663.2:g.150346427A>T	GRCh38
NC_000001.10:g.150318903A>T , CM000663.1:g.150318903A>T	GRCh37
NC_000001.9:g.148585527A>T	NCBI36
NG_008245.1:g.29976A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324862.7:c.1779A>T MANE Select	ENSP00000315379.6:p.Lys593Asn
ENST00000324862.6:c.1779A>T	ENSP00000315379.6:p.Lys593Asn
ENST00000467329.5:n.2106A>T
ENST00000476970.1:n.888A>T
NM_004698.2:c.1779A>T	NP_004689.1:p.Lys593Asn
XM_011510128.1:c.1779A>T	XP_011508430.1:p.Lys593Asn
XM_011510129.1:c.1374A>T	XP_011508431.1:p.Lys458Asn
XM_011510130.1:c.1347A>T	XP_011508432.1:p.Lys449Asn
XR_241103.1:n.1762A>T
XR_921997.1:n.1762A>T
XR_921998.1:n.1876A>T
NM_001350529.1:c.1374A>T	NP_001337458.1:p.Lys458Asn
NM_004698.3:c.1779A>T	NP_004689.1:p.Lys593Asn
NR_146766.1:n.2010A>T
NR_146767.1:n.2106A>T
NR_146768.1:n.1952A>T
NR_146769.1:n.2005A>T
XM_011510130.3:c.1347A>T	XP_011508432.1:p.Lys449Asn
XM_017002790.1:c.1347A>T	XP_016858279.1:p.Lys449Asn
XR_001737536.2:n.1812A>T
XR_001737537.2:n.1926A>T
XR_001737540.2:n.2683A>T
XR_001737541.2:n.1706A>T
XR_002958009.1:n.2436A>T
XR_002958010.1:n.3672A>T
XR_002958012.1:n.1868A>T
XR_241103.3:n.1754A>T
XR_921997.3:n.1754A>T
XR_921998.3:n.1868A>T
NM_004698.4:c.1779A>T MANE Select	NP_004689.1:p.Lys593Asn