Canonical Allele Identifier: CA394803174

Gene: PARN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.14584760G>A , CM000678.2:g.14584760G>A	GRCh38
NC_000016.9:g.14678617G>A , CM000678.1:g.14678617G>A	GRCh37
NC_000016.8:g.14586118G>A	NCBI36
NG_042871.1:g.50512C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_002582.4:c.994C>T MANE Select	NP_002573.1:p.Gln332Ter
ENST00000437198.7:c.994C>T MANE Select	ENSP00000387911.2:p.Gln332Ter
NM_001134477.2:c.811C>T	NP_001127949.1:p.Gln271Ter
NM_001134477.3:c.811C>T	NP_001127949.1:p.Gln271Ter
NM_001242992.1:c.856C>T	NP_001229921.1:p.Gln286Ter
NM_001242992.2:c.856C>T	NP_001229921.1:p.Gln286Ter
NM_002582.3:c.994C>T	NP_002573.1:p.Gln332Ter
ENST00000341484.11:c.811C>T	ENSP00000345456.7:p.Gln271Ter
ENST00000420015.6:c.856C>T	ENSP00000410525.2:p.Gln286Ter
ENST00000437198.6:c.994C>T	ENSP00000387911.2:p.Gln332Ter
ENST00000539279.5:c.469C>T	ENSP00000444381.1:p.Gln157Ter
ENST00000562715.1:n.32C>T
ENST00000563641.6:c.*758C>T	ENSP00000458103.1:n.*758C>T
ENST00000563697.5:n.1C>T
ENST00000564113.5:n.241C>T
ENST00000564113.6:n.1104C>T
ENST00000569444.5:c.459C>T
ENST00000650960.1:c.994C>T	ENSP00000499110.1:p.Gln332Ter
ENST00000650990.1:c.1069C>T	ENSP00000498741.1:p.Gln357Ter
ENST00000651027.1:c.994C>T	ENSP00000498640.1:p.Gln332Ter
ENST00000651049.1:c.994C>T	ENSP00000498644.1:p.Gln332Ter
ENST00000651300.1:c.*888C>T	ENSP00000498294.1:n.*888C>T
ENST00000651348.1:c.*65C>T	ENSP00000498315.1:n.*65C>T
ENST00000651634.1:c.994C>T	ENSP00000499078.1:p.Gln332Ter
ENST00000651760.1:c.2182C>T
ENST00000651865.1:c.919C>T	ENSP00000498567.1:p.Gln307Ter
ENST00000651913.1:c.941C>T
ENST00000652051.1:c.994C>T	ENSP00000498898.1:p.Gln332Ter
ENST00000652066.1:c.774C>T
ENST00000652411.1:n.1151C>T
ENST00000652501.1:c.994C>T	ENSP00000498261.1:p.Gln332Ter
ENST00000652541.1:c.*728C>T	ENSP00000499206.1:n.*728C>T
ENST00000652727.1:c.919-338C>T	ENSP00000498650.1:n.919-338C>T
ENST00000697471.1:n.1445C>T
ENST00000697472.1:n.1035C>T
ENST00000697473.1:n.2608-338C>T
ENST00000697474.1:c.994C>T	ENSP00000513329.1:p.Gln332Ter
ENST00000697475.1:n.1149C>T
ENST00000697476.1:n.1127C>T
XM_011522510.1:c.994C>T	XP_011520812.1:p.Gln332Ter
XM_011522510.3:c.994C>T	XP_011520812.1:p.Gln332Ter
XM_011522511.1:c.994C>T	XP_011520813.1:p.Gln332Ter
XM_011522511.2:c.994C>T	XP_011520813.1:p.Gln332Ter
XM_011522512.1:c.994C>T	XP_011520814.1:p.Gln332Ter
XM_011522513.1:c.811C>T	XP_011520815.1:p.Gln271Ter
XM_011522513.2:c.811C>T	XP_011520815.1:p.Gln271Ter
XM_011522514.1:c.994C>T	XP_011520816.1:p.Gln332Ter
XM_011522514.2:c.994C>T	XP_011520816.1:p.Gln332Ter
XM_017023258.2:c.916C>T	XP_016878747.1:p.Gln306Ter
XM_017023259.2:c.157C>T	XP_016878748.1:p.Gln53Ter
XM_017023260.1:c.157C>T	XP_016878749.1:p.Gln53Ter
XM_024450292.1:c.157C>T	XP_024306060.1:p.Gln53Ter
XR_001751906.2:n.1111C>T
XR_001751907.2:n.1111C>T