Canonical Allele Identifier: CA394804812

Gene: PARN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.14593380T>C , CM000678.2:g.14593380T>C	GRCh38
NC_000016.9:g.14687237T>C , CM000678.1:g.14687237T>C	GRCh37
NC_000016.8:g.14594738T>C	NCBI36
NG_042871.1:g.41892A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_002582.4:c.841-2A>G MANE Select	NP_002573.1:n.841-2A>G
ENST00000437198.7:c.841-2A>G MANE Select	ENSP00000387911.2:n.841-2A>G
NM_001134477.2:c.658-2A>G	NP_001127949.1:n.658-2A>G
NM_001134477.3:c.658-2A>G	NP_001127949.1:n.658-2A>G
NM_001242992.1:c.703-2A>G	NP_001229921.1:n.703-2A>G
NM_001242992.2:c.703-2A>G	NP_001229921.1:n.703-2A>G
NM_002582.3:c.841-2A>G	NP_002573.1:n.841-2A>G
ENST00000341484.11:c.658-2A>G	ENSP00000345456.7:n.658-2A>G
ENST00000420015.6:c.703-2A>G	ENSP00000410525.2:n.703-2A>G
ENST00000437198.6:c.841-2A>G	ENSP00000387911.2:n.841-2A>G
ENST00000539279.5:c.316-2A>G	ENSP00000444381.1:n.316-2A>G
ENST00000563641.5:c.*575-2A>G	ENSP00000458103.1:n.*575-2A>G
ENST00000563641.6:c.*605-2A>G	ENSP00000458103.1:n.*605-2A>G
ENST00000564113.6:n.951-2A>G
ENST00000569444.5:c.306-2A>G
ENST00000650960.1:c.841-2A>G	ENSP00000499110.1:n.841-2A>G
ENST00000650990.1:c.841-2A>G	ENSP00000498741.1:n.841-2A>G
ENST00000651027.1:c.841-2A>G	ENSP00000498640.1:n.841-2A>G
ENST00000651049.1:c.841-2A>G	ENSP00000498644.1:n.841-2A>G
ENST00000651241.1:n.1867-2A>G
ENST00000651300.1:c.*735-2A>G	ENSP00000498294.1:n.*735-2A>G
ENST00000651348.1:c.841-2A>G	ENSP00000498315.1:n.841-2A>G
ENST00000651634.1:c.841-2A>G	ENSP00000499078.1:n.841-2A>G
ENST00000651760.1:c.641-2A>G
ENST00000651865.1:c.691-2A>G	ENSP00000498567.1:n.691-2A>G
ENST00000651913.1:c.788-2A>G
ENST00000652051.1:c.841-2A>G	ENSP00000498898.1:n.841-2A>G
ENST00000652066.1:c.546-2A>G
ENST00000652411.1:n.998-2A>G
ENST00000652501.1:c.841-2A>G	ENSP00000498261.1:n.841-2A>G
ENST00000652541.1:c.*575-2A>G	ENSP00000499206.1:n.*575-2A>G
ENST00000652727.1:c.841-2A>G	ENSP00000498650.1:n.841-2A>G
ENST00000697471.1:n.1292-2A>G
ENST00000697472.1:n.882-2A>G
ENST00000697473.1:n.2486-2A>G
ENST00000697474.1:c.841-2A>G	ENSP00000513329.1:n.841-2A>G
ENST00000697475.1:n.996-2A>G
ENST00000697476.1:n.974-2A>G
XM_011522510.1:c.841-2A>G	XP_011520812.1:n.841-2A>G
XM_011522510.3:c.841-2A>G	XP_011520812.1:n.841-2A>G
XM_011522511.1:c.841-2A>G	XP_011520813.1:n.841-2A>G
XM_011522511.2:c.841-2A>G	XP_011520813.1:n.841-2A>G
XM_011522512.1:c.841-2A>G	XP_011520814.1:n.841-2A>G
XM_011522513.1:c.658-2A>G	XP_011520815.1:n.658-2A>G
XM_011522513.2:c.658-2A>G	XP_011520815.1:n.658-2A>G
XM_011522514.1:c.841-2A>G	XP_011520816.1:n.841-2A>G
XM_011522514.2:c.841-2A>G	XP_011520816.1:n.841-2A>G
XM_017023258.2:c.840+6524A>G	XP_016878747.1:n.840+6524A>G
XM_017023259.2:c.48-2A>G	XP_016878748.1:n.48-2A>G
XM_017023260.1:c.48-2A>G	XP_016878749.1:n.48-2A>G
XM_024450292.1:c.48-2A>G	XP_024306060.1:n.48-2A>G
XR_001751906.2:n.1002-2A>G
XR_001751907.2:n.1002-2A>G