Canonical Allele Identifier: CA395183735

Gene: PARN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.14482828C>T , CM000678.2:g.14482828C>T	GRCh38
NC_000016.9:g.14576685C>T , CM000678.1:g.14576685C>T	GRCh37
NC_000016.8:g.14484186C>T	NCBI36
NG_042871.1:g.152444G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002582.4:c.1481-1G>A MANE Select	NP_002573.1:n.1481-1G>A
ENST00000437198.7:c.1481-1G>A MANE Select	ENSP00000387911.2:n.1481-1G>A
NM_001134477.2:c.1298-1G>A	NP_001127949.1:n.1298-1G>A
NM_001134477.3:c.1298-1G>A	NP_001127949.1:n.1298-1G>A
NM_001242992.1:c.1343-1G>A	NP_001229921.1:n.1343-1G>A
NM_001242992.2:c.1343-1G>A	NP_001229921.1:n.1343-1G>A
NM_002582.3:c.1481-1G>A	NP_002573.1:n.1481-1G>A
ENST00000341484.11:c.1298-1G>A	ENSP00000345456.7:n.1298-1G>A
ENST00000420015.6:c.1343-1G>A	ENSP00000410525.2:n.1343-1G>A
ENST00000437198.6:c.1481-1G>A	ENSP00000387911.2:n.1481-1G>A
ENST00000539279.5:c.956-1G>A	ENSP00000444381.1:n.956-1G>A
ENST00000564113.6:n.1591-1G>A
ENST00000564882.5:n.138-1G>A
ENST00000564904.5:n.279-1G>A
ENST00000650960.1:c.1481-1G>A	ENSP00000499110.1:n.1481-1G>A
ENST00000650990.1:c.1556-1G>A	ENSP00000498741.1:n.1556-1G>A
ENST00000651049.1:c.1481-1G>A	ENSP00000498644.1:n.1481-1G>A
ENST00000651300.1:c.*1288-1G>A	ENSP00000498294.1:n.*1288-1G>A
ENST00000651348.1:c.*552-1G>A	ENSP00000498315.1:n.*552-1G>A
ENST00000651634.1:c.1481-1G>A	ENSP00000499078.1:n.1481-1G>A
ENST00000651760.1:c.2669-1G>A
ENST00000651865.1:c.1406-1G>A	ENSP00000498567.1:n.1406-1G>A
ENST00000652051.1:c.*257-1G>A	ENSP00000498898.1:n.*257-1G>A
ENST00000652066.1:c.1382-1G>A
ENST00000652541.1:c.*1313-1G>A	ENSP00000499206.1:n.*1313-1G>A
ENST00000652727.1:c.1307-1G>A	ENSP00000498650.1:n.1307-1G>A
ENST00000697471.1:n.1932-1G>A
ENST00000697472.1:n.1522-1G>A
ENST00000697473.1:n.3083-1G>A
ENST00000697474.1:c.1481-1G>A	ENSP00000513329.1:n.1481-1G>A
XM_011522510.1:c.1481-1G>A	XP_011520812.1:n.1481-1G>A
XM_011522510.3:c.1481-1G>A	XP_011520812.1:n.1481-1G>A
XM_011522511.1:c.1481-1G>A	XP_011520813.1:n.1481-1G>A
XM_011522511.2:c.1481-1G>A	XP_011520813.1:n.1481-1G>A
XM_011522512.1:c.1394-1G>A	XP_011520814.1:n.1394-1G>A
XM_011522513.1:c.1298-1G>A	XP_011520815.1:n.1298-1G>A
XM_011522513.2:c.1298-1G>A	XP_011520815.1:n.1298-1G>A
XM_017023258.2:c.1403-1G>A	XP_016878747.1:n.1403-1G>A
XM_017023259.2:c.644-1G>A	XP_016878748.1:n.644-1G>A
XM_017023260.1:c.644-1G>A	XP_016878749.1:n.644-1G>A
XM_024450292.1:c.644-1G>A	XP_024306060.1:n.644-1G>A
XR_001751906.2:n.1598-1G>A