Canonical Allele Identifier: CA7912411

Gene: PARN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.14610732C>A , CM000678.2:g.14610732C>A	GRCh38
NC_000016.9:g.14704589C>A , CM000678.1:g.14704589C>A	GRCh37
NC_000016.8:g.14612090C>A	NCBI36
NG_042871.1:g.24540G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_002582.4:c.466G>T MANE Select	NP_002573.1:p.Ala156Ser
ENST00000437198.7:c.466G>T MANE Select	ENSP00000387911.2:p.Ala156Ser
NM_001134477.2:c.283G>T	NP_001127949.1:p.Ala95Ser
NM_001134477.3:c.283G>T	NP_001127949.1:p.Ala95Ser
NM_001242992.1:c.328G>T	NP_001229921.1:p.Ala110Ser
NM_001242992.2:c.328G>T	NP_001229921.1:p.Ala110Ser
NM_002582.3:c.466G>T	NP_002573.1:p.Ala156Ser
ENST00000341484.11:c.283G>T	ENSP00000345456.7:p.Ala95Ser
ENST00000420015.6:c.328G>T	ENSP00000410525.2:p.Ala110Ser
ENST00000437198.6:c.466G>T	ENSP00000387911.2:p.Ala156Ser
ENST00000538472.5:c.415G>T	ENSP00000445659.1:p.Ala139Ser
ENST00000539279.5:c.178-6506G>T	ENSP00000444381.1:n.178-6506G>T
ENST00000563641.5:c.*200G>T	ENSP00000458103.1:n.*200G>T
ENST00000563641.6:c.*230G>T	ENSP00000458103.1:n.*230G>T
ENST00000564113.6:n.576G>T
ENST00000566021.1:n.531G>T
ENST00000569444.5:c.12G>T
ENST00000650960.1:c.466G>T	ENSP00000499110.1:p.Ala156Ser
ENST00000650990.1:c.466G>T	ENSP00000498741.1:p.Ala156Ser
ENST00000651027.1:c.466G>T	ENSP00000498640.1:p.Ala156Ser
ENST00000651049.1:c.466G>T	ENSP00000498644.1:p.Ala156Ser
ENST00000651241.1:n.1492G>T
ENST00000651300.1:c.*360G>T	ENSP00000498294.1:n.*360G>T
ENST00000651348.1:c.466G>T	ENSP00000498315.1:p.Ala156Ser
ENST00000651634.1:c.466G>T	ENSP00000499078.1:p.Ala156Ser
ENST00000651760.1:c.266G>T
ENST00000651865.1:c.316G>T	ENSP00000498567.1:p.Ala106Ser
ENST00000651913.1:c.416G>T
ENST00000652051.1:c.466G>T	ENSP00000498898.1:p.Ala156Ser
ENST00000652066.1:c.171G>T
ENST00000652411.1:n.623G>T
ENST00000652501.1:c.466G>T	ENSP00000498261.1:p.Ala156Ser
ENST00000652541.1:c.*200G>T	ENSP00000499206.1:n.*200G>T
ENST00000652727.1:c.466G>T	ENSP00000498650.1:p.Ala156Ser
ENST00000697471.1:n.917G>T
ENST00000697472.1:n.612G>T
ENST00000697473.1:n.591G>T
ENST00000697474.1:c.466G>T	ENSP00000513329.1:p.Ala156Ser
ENST00000697475.1:n.621G>T
ENST00000697476.1:n.599G>T
ENST00000697477.1:n.601G>T
XM_011522510.1:c.466G>T	XP_011520812.1:p.Ala156Ser
XM_011522510.3:c.466G>T	XP_011520812.1:p.Ala156Ser
XM_011522511.1:c.466G>T	XP_011520813.1:p.Ala156Ser
XM_011522511.2:c.466G>T	XP_011520813.1:p.Ala156Ser
XM_011522512.1:c.466G>T	XP_011520814.1:p.Ala156Ser
XM_011522513.1:c.283G>T	XP_011520815.1:p.Ala95Ser
XM_011522513.2:c.283G>T	XP_011520815.1:p.Ala95Ser
XM_011522514.1:c.466G>T	XP_011520816.1:p.Ala156Ser
XM_011522514.2:c.466G>T	XP_011520816.1:p.Ala156Ser
XM_017023258.2:c.466G>T	XP_016878747.1:p.Ala156Ser
XM_017023259.2:c.-328G>T	XP_016878748.1:n.-328G>T
XM_017023260.1:c.-328G>T	XP_016878749.1:n.-328G>T
XM_024450292.1:c.-1066G>T	XP_024306060.1:n.-1066G>T
XR_001751906.2:n.627G>T
XR_001751907.2:n.627G>T