Canonical Allele Identifier: CA394804739

Gene: PARN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.14593360G>A , CM000678.2:g.14593360G>A	GRCh38
NC_000016.9:g.14687217G>A , CM000678.1:g.14687217G>A	GRCh37
NC_000016.8:g.14594718G>A	NCBI36
NG_042871.1:g.41912C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697471.1:n.1310C>T
ENST00000697472.1:n.900C>T
ENST00000697473.1:n.2504C>T
ENST00000697474.1:c.859C>T	ENSP00000513329.1:p.His287Tyr
ENST00000697475.1:n.1014C>T
ENST00000697476.1:n.992C>T
ENST00000437198.7:c.859C>T MANE Select	ENSP00000387911.2:p.His287Tyr
ENST00000563641.6:c.*623C>T	ENSP00000458103.1:n.*623C>T
ENST00000564113.6:n.969C>T
ENST00000650960.1:c.859C>T	ENSP00000499110.1:p.His287Tyr
ENST00000650990.1:c.859C>T	ENSP00000498741.1:p.His287Tyr
ENST00000651027.1:c.859C>T	ENSP00000498640.1:p.His287Tyr
ENST00000651049.1:c.859C>T	ENSP00000498644.1:p.His287Tyr
ENST00000651241.1:n.1885C>T
ENST00000651300.1:c.*753C>T	ENSP00000498294.1:n.*753C>T
ENST00000651348.1:c.859C>T	ENSP00000498315.1:p.His287Tyr
ENST00000651634.1:c.859C>T	ENSP00000499078.1:p.His287Tyr
ENST00000651760.1:c.659C>T
ENST00000651865.1:c.709C>T	ENSP00000498567.1:p.His237Tyr
ENST00000651913.1:c.806C>T
ENST00000652051.1:c.859C>T	ENSP00000498898.1:p.His287Tyr
ENST00000652066.1:c.564C>T
ENST00000652411.1:n.1016C>T
ENST00000652501.1:c.859C>T	ENSP00000498261.1:p.His287Tyr
ENST00000652541.1:c.*593C>T	ENSP00000499206.1:n.*593C>T
ENST00000652727.1:c.859C>T	ENSP00000498650.1:p.His287Tyr
ENST00000341484.11:c.676C>T	ENSP00000345456.7:p.His226Tyr
ENST00000420015.6:c.721C>T	ENSP00000410525.2:p.His241Tyr
ENST00000437198.6:c.859C>T	ENSP00000387911.2:p.His287Tyr
ENST00000539279.5:c.334C>T	ENSP00000444381.1:p.His112Tyr
ENST00000563641.5:c.*593C>T	ENSP00000458103.1:n.*593C>T
ENST00000569444.5:c.324C>T
NM_001134477.2:c.676C>T	NP_001127949.1:p.His226Tyr
NM_001242992.1:c.721C>T	NP_001229921.1:p.His241Tyr
NM_002582.3:c.859C>T	NP_002573.1:p.His287Tyr
XM_011522510.1:c.859C>T	XP_011520812.1:p.His287Tyr
XM_011522511.1:c.859C>T	XP_011520813.1:p.His287Tyr
XM_011522512.1:c.859C>T	XP_011520814.1:p.His287Tyr
XM_011522513.1:c.676C>T	XP_011520815.1:p.His226Tyr
XM_011522514.1:c.859C>T	XP_011520816.1:p.His287Tyr
NM_002582.4:c.859C>T MANE Select	NP_002573.1:p.His287Tyr
XM_011522510.3:c.859C>T	XP_011520812.1:p.His287Tyr
XM_011522511.2:c.859C>T	XP_011520813.1:p.His287Tyr
XM_011522513.2:c.676C>T	XP_011520815.1:p.His226Tyr
XM_011522514.2:c.859C>T	XP_011520816.1:p.His287Tyr
XM_017023258.2:c.840+6544C>T	XP_016878747.1:n.840+6544C>T
XM_017023259.2:c.66C>T	XP_016878748.1:p.Asp22=
XM_017023260.1:c.66C>T	XP_016878749.1:p.Asp22=
XM_024450292.1:c.66C>T	XP_024306060.1:p.Asp22=
XR_001751906.2:n.1020C>T
XR_001751907.2:n.1020C>T
NM_001134477.3:c.676C>T	NP_001127949.1:p.His226Tyr
NM_001242992.2:c.721C>T	NP_001229921.1:p.His241Tyr