Canonical Allele Identifier: CA278511103

Gene: PARN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.14584499dup , CM000678.2:g.14584499dup	GRCh38
NC_000016.9:g.14678356dup , CM000678.1:g.14678356dup	GRCh37
NC_000016.8:g.14585857dup	NCBI36
NG_042871.1:g.50779dup

Transcript Alleles

HGVS	Amino-acid Change
NM_002582.4:c.1006-71dup MANE Select	NP_002573.1:n.1006-71dup
ENST00000437198.7:c.1006-71dup MANE Select	ENSP00000387911.2:n.1006-71dup
NM_001134477.2:c.823-71dup	NP_001127949.1:n.823-71dup
NM_001134477.3:c.823-71dup	NP_001127949.1:n.823-71dup
NM_001242992.1:c.868-71dup	NP_001229921.1:n.868-71dup
NM_001242992.2:c.868-71dup	NP_001229921.1:n.868-71dup
NM_002582.3:c.1006-71dup	NP_002573.1:n.1006-71dup
ENST00000341484.11:c.823-71dup	ENSP00000345456.7:n.823-71dup
ENST00000420015.6:c.868-71dup	ENSP00000410525.2:n.868-71dup
ENST00000437198.6:c.1006-71dup	ENSP00000387911.2:n.1006-71dup
ENST00000539279.5:c.481-71dup	ENSP00000444381.1:n.481-71dup
ENST00000562715.1:n.44-71dup
ENST00000563641.6:c.*770-71dup	ENSP00000458103.1:n.*770-71dup
ENST00000563697.5:n.13-71dup
ENST00000564113.5:n.253-71dup
ENST00000564113.6:n.1116-71dup
ENST00000569444.5:c.471-71dup
ENST00000650960.1:c.1006-71dup	ENSP00000499110.1:n.1006-71dup
ENST00000650990.1:c.1081-71dup	ENSP00000498741.1:n.1081-71dup
ENST00000651027.1:c.1006-71dup	ENSP00000498640.1:n.1006-71dup
ENST00000651049.1:c.1006-71dup	ENSP00000498644.1:n.1006-71dup
ENST00000651300.1:c.*900-71dup	ENSP00000498294.1:n.*900-71dup
ENST00000651348.1:c.*77-71dup	ENSP00000498315.1:n.*77-71dup
ENST00000651634.1:c.1006-71dup	ENSP00000499078.1:n.1006-71dup
ENST00000651760.1:c.2194-71dup
ENST00000651865.1:c.931-71dup	ENSP00000498567.1:n.931-71dup
ENST00000651913.1:c.953-71dup
ENST00000652051.1:c.1006-71dup	ENSP00000498898.1:n.1006-71dup
ENST00000652066.1:c.786-71dup
ENST00000652411.1:n.1163-71dup
ENST00000652501.1:c.1006-71dup	ENSP00000498261.1:n.1006-71dup
ENST00000652541.1:c.*740-71dup	ENSP00000499206.1:n.*740-71dup
ENST00000652727.1:c.919-71dup	ENSP00000498650.1:n.919-71dup
ENST00000697471.1:n.1457-71dup
ENST00000697472.1:n.1047-71dup
ENST00000697473.1:n.2608-71dup
ENST00000697474.1:c.1006-71dup	ENSP00000513329.1:n.1006-71dup
ENST00000697475.1:n.1161-71dup
ENST00000697476.1:n.1139-71dup
XM_011522510.1:c.1006-71dup	XP_011520812.1:n.1006-71dup
XM_011522510.3:c.1006-71dup	XP_011520812.1:n.1006-71dup
XM_011522511.1:c.1006-71dup	XP_011520813.1:n.1006-71dup
XM_011522511.2:c.1006-71dup	XP_011520813.1:n.1006-71dup
XM_011522512.1:c.1006-71dup	XP_011520814.1:n.1006-71dup
XM_011522513.1:c.823-71dup	XP_011520815.1:n.823-71dup
XM_011522513.2:c.823-71dup	XP_011520815.1:n.823-71dup
XM_011522514.1:c.1006-71dup	XP_011520816.1:n.1006-71dup
XM_011522514.2:c.1006-71dup	XP_011520816.1:n.1006-71dup
XM_017023258.2:c.928-71dup	XP_016878747.1:n.928-71dup
XM_017023259.2:c.169-71dup	XP_016878748.1:n.169-71dup
XM_017023260.1:c.169-71dup	XP_016878749.1:n.169-71dup
XM_024450292.1:c.169-71dup	XP_024306060.1:n.169-71dup
XR_001751906.2:n.1123-71dup
XR_001751907.2:n.1123-71dup