Canonical Allele Identifier: CA278533003

Gene: PARN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.14608985T>C , CM000678.2:g.14608985T>C	GRCh38
NC_000016.9:g.14702842T>C , CM000678.1:g.14702842T>C	GRCh37
NC_000016.8:g.14610343T>C	NCBI36
NG_042871.1:g.26287A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_002582.4:c.620+73A>G MANE Select	NP_002573.1:n.620+73A>G
ENST00000437198.7:c.620+73A>G MANE Select	ENSP00000387911.2:n.620+73A>G
NM_001134477.2:c.437+73A>G	NP_001127949.1:n.437+73A>G
NM_001134477.3:c.437+73A>G	NP_001127949.1:n.437+73A>G
NM_001242992.1:c.482+73A>G	NP_001229921.1:n.482+73A>G
NM_001242992.2:c.482+73A>G	NP_001229921.1:n.482+73A>G
NM_002582.3:c.620+73A>G	NP_002573.1:n.620+73A>G
ENST00000341484.11:c.437+73A>G	ENSP00000345456.7:n.437+73A>G
ENST00000420015.6:c.482+73A>G	ENSP00000410525.2:n.482+73A>G
ENST00000437198.6:c.620+73A>G	ENSP00000387911.2:n.620+73A>G
ENST00000538472.5:c.569+73A>G	ENSP00000445659.1:n.569+73A>G
ENST00000539279.5:c.178-4759A>G	ENSP00000444381.1:n.178-4759A>G
ENST00000563155.1:n.122+73A>G
ENST00000563641.5:c.*354+73A>G	ENSP00000458103.1:n.*354+73A>G
ENST00000563641.6:c.*384+73A>G	ENSP00000458103.1:n.*384+73A>G
ENST00000564113.6:n.730+73A>G
ENST00000569444.5:c.166+73A>G
ENST00000650960.1:c.620+73A>G	ENSP00000499110.1:n.620+73A>G
ENST00000650990.1:c.620+73A>G	ENSP00000498741.1:n.620+73A>G
ENST00000651027.1:c.620+73A>G	ENSP00000498640.1:n.620+73A>G
ENST00000651049.1:c.620+73A>G	ENSP00000498644.1:n.620+73A>G
ENST00000651241.1:n.1646+73A>G
ENST00000651300.1:c.*514+73A>G	ENSP00000498294.1:n.*514+73A>G
ENST00000651348.1:c.620+73A>G	ENSP00000498315.1:n.620+73A>G
ENST00000651634.1:c.620+73A>G	ENSP00000499078.1:n.620+73A>G
ENST00000651760.1:c.420+73A>G
ENST00000651865.1:c.470+73A>G	ENSP00000498567.1:n.470+73A>G
ENST00000651913.1:c.570+73A>G
ENST00000652051.1:c.620+73A>G	ENSP00000498898.1:n.620+73A>G
ENST00000652066.1:c.325+73A>G
ENST00000652411.1:n.777+73A>G
ENST00000652501.1:c.620+73A>G	ENSP00000498261.1:n.620+73A>G
ENST00000652541.1:c.*354+73A>G	ENSP00000499206.1:n.*354+73A>G
ENST00000652727.1:c.620+73A>G	ENSP00000498650.1:n.620+73A>G
ENST00000697471.1:n.1071+73A>G
ENST00000697472.1:n.700+1659A>G
ENST00000697473.1:n.2265+73A>G
ENST00000697474.1:c.620+73A>G	ENSP00000513329.1:n.620+73A>G
ENST00000697475.1:n.775+73A>G
ENST00000697476.1:n.753+73A>G
ENST00000697477.1:n.755+73A>G
XM_011522510.1:c.620+73A>G	XP_011520812.1:n.620+73A>G
XM_011522510.3:c.620+73A>G	XP_011520812.1:n.620+73A>G
XM_011522511.1:c.620+73A>G	XP_011520813.1:n.620+73A>G
XM_011522511.2:c.620+73A>G	XP_011520813.1:n.620+73A>G
XM_011522512.1:c.620+73A>G	XP_011520814.1:n.620+73A>G
XM_011522513.1:c.437+73A>G	XP_011520815.1:n.437+73A>G
XM_011522513.2:c.437+73A>G	XP_011520815.1:n.437+73A>G
XM_011522514.1:c.620+73A>G	XP_011520816.1:n.620+73A>G
XM_011522514.2:c.620+73A>G	XP_011520816.1:n.620+73A>G
XM_017023258.2:c.620+73A>G	XP_016878747.1:n.620+73A>G
XM_017023259.2:c.-174+73A>G	XP_016878748.1:n.-174+73A>G
XM_017023260.1:c.-174+73A>G	XP_016878749.1:n.-174+73A>G
XM_024450292.1:c.-839A>G	XP_024306060.1:n.-839A>G
XR_001751906.2:n.781+73A>G
XR_001751907.2:n.781+73A>G