Canonical Allele Identifier: CA278533814

Gene: PARN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.14581061T>C , CM000678.2:g.14581061T>C	GRCh38
NC_000016.9:g.14674918T>C , CM000678.1:g.14674918T>C	GRCh37
NC_000016.8:g.14582419T>C	NCBI36
NG_042871.1:g.54211A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_002582.4:c.1193-118A>G MANE Select	NP_002573.1:n.1193-118A>G
ENST00000437198.7:c.1193-118A>G MANE Select	ENSP00000387911.2:n.1193-118A>G
NM_001134477.2:c.1010-118A>G	NP_001127949.1:n.1010-118A>G
NM_001134477.3:c.1010-118A>G	NP_001127949.1:n.1010-118A>G
NM_001242992.1:c.1055-118A>G	NP_001229921.1:n.1055-118A>G
NM_001242992.2:c.1055-118A>G	NP_001229921.1:n.1055-118A>G
NM_002582.3:c.1193-118A>G	NP_002573.1:n.1193-118A>G
ENST00000341484.11:c.1010-118A>G	ENSP00000345456.7:n.1010-118A>G
ENST00000420015.6:c.1055-118A>G	ENSP00000410525.2:n.1055-118A>G
ENST00000437198.6:c.1193-118A>G	ENSP00000387911.2:n.1193-118A>G
ENST00000539279.5:c.668-118A>G	ENSP00000444381.1:n.668-118A>G
ENST00000562715.1:n.231-118A>G
ENST00000563641.6:c.*957-118A>G	ENSP00000458103.1:n.*957-118A>G
ENST00000563697.5:n.200-118A>G
ENST00000564113.5:n.440-118A>G
ENST00000564113.6:n.1303-118A>G
ENST00000569444.5:c.658-118A>G
ENST00000650960.1:c.1193-118A>G	ENSP00000499110.1:n.1193-118A>G
ENST00000650990.1:c.1268-118A>G	ENSP00000498741.1:n.1268-118A>G
ENST00000651027.1:c.1193-118A>G	ENSP00000498640.1:n.1193-118A>G
ENST00000651049.1:c.1193-118A>G	ENSP00000498644.1:n.1193-118A>G
ENST00000651300.1:c.*1087-118A>G	ENSP00000498294.1:n.*1087-118A>G
ENST00000651348.1:c.*264-118A>G	ENSP00000498315.1:n.*264-118A>G
ENST00000651634.1:c.1193-118A>G	ENSP00000499078.1:n.1193-118A>G
ENST00000651760.1:c.2381-118A>G
ENST00000651865.1:c.1118-118A>G	ENSP00000498567.1:n.1118-118A>G
ENST00000651913.1:c.1140-118A>G
ENST00000652051.1:c.1193-118A>G	ENSP00000498898.1:n.1193-118A>G
ENST00000652066.1:c.973-118A>G
ENST00000652411.1:n.1350-118A>G
ENST00000652501.1:c.1193-118A>G	ENSP00000498261.1:n.1193-118A>G
ENST00000652541.1:c.*927-118A>G	ENSP00000499206.1:n.*927-118A>G
ENST00000652727.1:c.1106-118A>G	ENSP00000498650.1:n.1106-118A>G
ENST00000697471.1:n.1644-118A>G
ENST00000697472.1:n.1234-118A>G
ENST00000697473.1:n.2795-118A>G
ENST00000697474.1:c.1193-118A>G	ENSP00000513329.1:n.1193-118A>G
ENST00000697475.1:n.1348-118A>G
ENST00000697476.1:n.1326-118A>G
XM_011522510.1:c.1193-118A>G	XP_011520812.1:n.1193-118A>G
XM_011522510.3:c.1193-118A>G	XP_011520812.1:n.1193-118A>G
XM_011522511.1:c.1193-118A>G	XP_011520813.1:n.1193-118A>G
XM_011522511.2:c.1193-118A>G	XP_011520813.1:n.1193-118A>G
XM_011522512.1:c.1193-118A>G	XP_011520814.1:n.1193-118A>G
XM_011522513.1:c.1010-118A>G	XP_011520815.1:n.1010-118A>G
XM_011522513.2:c.1010-118A>G	XP_011520815.1:n.1010-118A>G
XM_011522514.1:c.1193-118A>G	XP_011520816.1:n.1193-118A>G
XM_011522514.2:c.1193-118A>G	XP_011520816.1:n.1193-118A>G
XM_017023258.2:c.1115-118A>G	XP_016878747.1:n.1115-118A>G
XM_017023259.2:c.356-118A>G	XP_016878748.1:n.356-118A>G
XM_017023260.1:c.356-118A>G	XP_016878749.1:n.356-118A>G
XM_024450292.1:c.356-118A>G	XP_024306060.1:n.356-118A>G
XR_001751906.2:n.1310-118A>G
XR_001751907.2:n.1310-118A>G