Canonical Allele Identifier: CA394813305

Gene: PARN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.14617652T>C , CM000678.2:g.14617652T>C	GRCh38
NC_000016.9:g.14711509T>C , CM000678.1:g.14711509T>C	GRCh37
NC_000016.8:g.14619010T>C	NCBI36
NG_042871.1:g.17620A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_002582.4:c.328-2A>G MANE Select	NP_002573.1:n.328-2A>G
ENST00000437198.7:c.328-2A>G MANE Select	ENSP00000387911.2:n.328-2A>G
NM_001134477.2:c.145-2A>G	NP_001127949.1:n.145-2A>G
NM_001134477.3:c.145-2A>G	NP_001127949.1:n.145-2A>G
NM_001242992.1:c.190-2A>G	NP_001229921.1:n.190-2A>G
NM_001242992.2:c.190-2A>G	NP_001229921.1:n.190-2A>G
NM_002582.3:c.328-2A>G	NP_002573.1:n.328-2A>G
ENST00000341484.11:c.145-2A>G	ENSP00000345456.7:n.145-2A>G
ENST00000420015.6:c.190-2A>G	ENSP00000410525.2:n.190-2A>G
ENST00000437198.6:c.328-2A>G	ENSP00000387911.2:n.328-2A>G
ENST00000538472.5:c.277-2A>G	ENSP00000445659.1:n.277-2A>G
ENST00000539279.5:c.177+10520A>G	ENSP00000444381.1:n.177+10520A>G
ENST00000563641.5:c.*62-2A>G	ENSP00000458103.1:n.*62-2A>G
ENST00000563641.6:c.*92-2A>G	ENSP00000458103.1:n.*92-2A>G
ENST00000564113.6:n.438-2A>G
ENST00000566021.1:n.454-6843A>G
ENST00000650960.1:c.328-2A>G	ENSP00000499110.1:n.328-2A>G
ENST00000650990.1:c.328-2A>G	ENSP00000498741.1:n.328-2A>G
ENST00000651027.1:c.328-2A>G	ENSP00000498640.1:n.328-2A>G
ENST00000651049.1:c.328-2A>G	ENSP00000498644.1:n.328-2A>G
ENST00000651241.1:n.1354-2A>G
ENST00000651300.1:c.*222-2A>G	ENSP00000498294.1:n.*222-2A>G
ENST00000651348.1:c.328-2A>G	ENSP00000498315.1:n.328-2A>G
ENST00000651634.1:c.328-2A>G	ENSP00000499078.1:n.328-2A>G
ENST00000651760.1:c.128-2A>G
ENST00000651865.1:c.178-2A>G	ENSP00000498567.1:n.178-2A>G
ENST00000651913.1:c.278-2A>G
ENST00000652051.1:c.328-2A>G	ENSP00000498898.1:n.328-2A>G
ENST00000652066.1:c.33-2A>G
ENST00000652411.1:n.485-2A>G
ENST00000652501.1:c.328-2A>G	ENSP00000498261.1:n.328-2A>G
ENST00000652541.1:c.*62-2A>G	ENSP00000499206.1:n.*62-2A>G
ENST00000652727.1:c.328-2A>G	ENSP00000498650.1:n.328-2A>G
ENST00000697472.1:n.474-2A>G
ENST00000697473.1:n.453-2A>G
ENST00000697474.1:c.328-2A>G	ENSP00000513329.1:n.328-2A>G
ENST00000697475.1:n.483-2A>G
ENST00000697476.1:n.461-2A>G
ENST00000697477.1:n.463-2A>G
XM_011522510.1:c.328-2A>G	XP_011520812.1:n.328-2A>G
XM_011522510.3:c.328-2A>G	XP_011520812.1:n.328-2A>G
XM_011522511.1:c.328-2A>G	XP_011520813.1:n.328-2A>G
XM_011522511.2:c.328-2A>G	XP_011520813.1:n.328-2A>G
XM_011522512.1:c.328-2A>G	XP_011520814.1:n.328-2A>G
XM_011522513.1:c.145-2A>G	XP_011520815.1:n.145-2A>G
XM_011522513.2:c.145-2A>G	XP_011520815.1:n.145-2A>G
XM_011522514.1:c.328-2A>G	XP_011520816.1:n.328-2A>G
XM_011522514.2:c.328-2A>G	XP_011520816.1:n.328-2A>G
XM_017023258.2:c.328-2A>G	XP_016878747.1:n.328-2A>G
XM_017023259.2:c.-466-2A>G	XP_016878748.1:n.-466-2A>G
XM_017023260.1:c.-405-6843A>G	XP_016878749.1:n.-405-6843A>G
XM_024450292.1:c.-1204-2A>G	XP_024306060.1:n.-1204-2A>G
XR_001751906.2:n.489-2A>G
XR_001751907.2:n.489-2A>G