Canonical Allele Identifier: CA2631856631

Gene: PARN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.14593296C>T , CM000678.2:g.14593296C>T	GRCh38
NC_000016.9:g.14687153C>T , CM000678.1:g.14687153C>T	GRCh37
NC_000016.8:g.14594654C>T	NCBI36
NG_042871.1:g.41976G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002582.4:c.918+5G>A MANE Select	NP_002573.1:n.918+5G>A
ENST00000437198.7:c.918+5G>A MANE Select	ENSP00000387911.2:n.918+5G>A
NM_001134477.2:c.735+5G>A	NP_001127949.1:n.735+5G>A
NM_001134477.3:c.735+5G>A	NP_001127949.1:n.735+5G>A
NM_001242992.1:c.780+5G>A	NP_001229921.1:n.780+5G>A
NM_001242992.2:c.780+5G>A	NP_001229921.1:n.780+5G>A
NM_002582.3:c.918+5G>A	NP_002573.1:n.918+5G>A
ENST00000341484.11:c.735+5G>A	ENSP00000345456.7:n.735+5G>A
ENST00000420015.6:c.780+5G>A	ENSP00000410525.2:n.780+5G>A
ENST00000437198.6:c.918+5G>A	ENSP00000387911.2:n.918+5G>A
ENST00000539279.5:c.393+5G>A	ENSP00000444381.1:n.393+5G>A
ENST00000563641.5:c.*652+5G>A	ENSP00000458103.1:n.*652+5G>A
ENST00000563641.6:c.*682+5G>A	ENSP00000458103.1:n.*682+5G>A
ENST00000564113.6:n.1028+5G>A
ENST00000569444.5:c.383+5G>A
ENST00000650960.1:c.918+5G>A	ENSP00000499110.1:n.918+5G>A
ENST00000650990.1:c.918+5G>A	ENSP00000498741.1:n.918+5G>A
ENST00000651027.1:c.918+5G>A	ENSP00000498640.1:n.918+5G>A
ENST00000651049.1:c.918+5G>A	ENSP00000498644.1:n.918+5G>A
ENST00000651241.1:n.1944+5G>A
ENST00000651300.1:c.*812+5G>A	ENSP00000498294.1:n.*812+5G>A
ENST00000651348.1:c.918+5G>A	ENSP00000498315.1:n.918+5G>A
ENST00000651634.1:c.918+5G>A	ENSP00000499078.1:n.918+5G>A
ENST00000651760.1:c.723G>A
ENST00000651865.1:c.768+5G>A	ENSP00000498567.1:n.768+5G>A
ENST00000651913.1:c.865+5G>A
ENST00000652051.1:c.918+5G>A	ENSP00000498898.1:n.918+5G>A
ENST00000652066.1:c.623+5G>A
ENST00000652411.1:n.1075+5G>A
ENST00000652501.1:c.918+5G>A	ENSP00000498261.1:n.918+5G>A
ENST00000652541.1:c.*652+5G>A	ENSP00000499206.1:n.*652+5G>A
ENST00000652727.1:c.918+5G>A	ENSP00000498650.1:n.918+5G>A
ENST00000697471.1:n.1369+5G>A
ENST00000697472.1:n.959+5G>A
ENST00000697473.1:n.2563+5G>A
ENST00000697474.1:c.918+5G>A	ENSP00000513329.1:n.918+5G>A
ENST00000697475.1:n.1073+5G>A
ENST00000697476.1:n.1051+5G>A
XM_011522510.1:c.918+5G>A	XP_011520812.1:n.918+5G>A
XM_011522510.3:c.918+5G>A	XP_011520812.1:n.918+5G>A
XM_011522511.1:c.918+5G>A	XP_011520813.1:n.918+5G>A
XM_011522511.2:c.918+5G>A	XP_011520813.1:n.918+5G>A
XM_011522512.1:c.918+5G>A	XP_011520814.1:n.918+5G>A
XM_011522513.1:c.735+5G>A	XP_011520815.1:n.735+5G>A
XM_011522513.2:c.735+5G>A	XP_011520815.1:n.735+5G>A
XM_011522514.1:c.918+5G>A	XP_011520816.1:n.918+5G>A
XM_011522514.2:c.918+5G>A	XP_011520816.1:n.918+5G>A
XM_017023258.2:c.840+6608G>A	XP_016878747.1:n.840+6608G>A
XM_017023259.2:c.125+5G>A	XP_016878748.1:n.125+5G>A
XM_017023260.1:c.125+5G>A	XP_016878749.1:n.125+5G>A
XM_024450292.1:c.125+5G>A	XP_024306060.1:n.125+5G>A
XR_001751906.2:n.1079+5G>A
XR_001751907.2:n.1079+5G>A