Canonical Allele Identifier: CA390314888

Gene: PAPLN

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.73254976G>A , CM000676.2:g.73254976G>A	GRCh38
NC_000014.8:g.73721684G>A , CM000676.1:g.73721684G>A	GRCh37
NC_000014.7:g.72791437G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001365906.3:c.1585G>A MANE Select	NP_001352835.1:p.Asp529Asn
ENST00000644200.2:c.1585G>A MANE Select	ENSP00000495882.2:p.Asp529Asn
NM_001365906.1:c.1585G>A	NP_001352835.1:p.Asp529Asn
NM_001365907.1:c.1585G>A	NP_001352836.1:p.Asp529Asn
NM_001365907.2:c.1585G>A	NP_001352836.1:p.Asp529Asn
NM_173462.3:c.1504G>A	NP_775733.3:p.Asp502Asn
NM_173462.4:c.1504G>A	NP_775733.3:p.Asp502Asn
NR_158677.1:n.1597G>A
NR_158677.2:n.1597G>A
NR_158678.1:n.1678G>A
NR_158678.2:n.1678G>A
ENST00000216658.9:c.1585G>A	ENSP00000216658.5:p.Asp529Asn
ENST00000340738.9:c.1504G>A	ENSP00000345395.5:p.Asp502Asn
ENST00000554301.5:c.1585G>A	ENSP00000451803.1:p.Asp529Asn
ENST00000555123.5:c.1504G>A	ENSP00000452455.1:p.Asp502Asn
ENST00000555445.5:c.1585G>A	ENSP00000451729.1:p.Asp529Asn
XM_011537290.1:c.1585G>A	XP_011535592.1:p.Asp529Asn
XM_011537290.3:c.1585G>A	XP_011535592.1:p.Asp529Asn
XM_011537291.1:c.1585G>A	XP_011535593.1:p.Asp529Asn
XM_011537291.3:c.1585G>A	XP_011535593.1:p.Asp529Asn
XM_011537292.1:c.1585G>A	XP_011535594.1:p.Asp529Asn
XM_011537292.3:c.1585G>A	XP_011535594.1:p.Asp529Asn
XM_011537293.1:c.1606G>A	XP_011535595.1:p.Asp536Asn
XM_011537293.3:c.1606G>A	XP_011535595.1:p.Asp536Asn
XM_011537294.1:c.1453G>A	XP_011535596.1:p.Asp485Asn
XM_011537294.3:c.1453G>A	XP_011535596.1:p.Asp485Asn
XM_011537295.1:c.1606G>A	XP_011535597.1:p.Asp536Asn
XM_011537295.3:c.1606G>A	XP_011535597.1:p.Asp536Asn
XM_011537296.1:c.1606G>A	XP_011535598.1:p.Asp536Asn
XM_011537296.2:c.1606G>A	XP_011535598.1:p.Asp536Asn
XM_017021749.2:c.1606G>A	XP_016877238.1:p.Asp536Asn
XR_429333.2:n.2796G>A
XR_429333.3:n.1606G>A