Canonical Allele Identifier: CA16620071

Gene: PARN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.14628177T>A , CM000678.2:g.14628177T>A	GRCh38
NC_000016.9:g.14722034T>A , CM000678.1:g.14722034T>A	GRCh37
NC_000016.8:g.14629535T>A	NCBI36
NG_042871.1:g.7095A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697472.1:n.318A>T
ENST00000697473.1:n.297A>T
ENST00000697474.1:c.172A>T	ENSP00000513329.1:p.Lys58Ter
ENST00000697475.1:n.327A>T
ENST00000697476.1:n.305A>T
ENST00000697477.1:n.307A>T
ENST00000437198.7:c.172A>T MANE Select	ENSP00000387911.2:p.Lys58Ter
ENST00000563641.6:c.172A>T	ENSP00000458103.1:p.Lys58Ter
ENST00000564113.6:n.282A>T
ENST00000650960.1:c.172A>T	ENSP00000499110.1:p.Lys58Ter
ENST00000650990.1:c.172A>T	ENSP00000498741.1:p.Lys58Ter
ENST00000651027.1:c.172A>T	ENSP00000498640.1:p.Lys58Ter
ENST00000651049.1:c.172A>T	ENSP00000498644.1:p.Lys58Ter
ENST00000651241.1:n.282A>T
ENST00000651300.1:c.172A>T	ENSP00000498294.1:p.Lys58Ter
ENST00000651348.1:c.172A>T	ENSP00000498315.1:p.Lys58Ter
ENST00000651634.1:c.172A>T	ENSP00000499078.1:p.Lys58Ter
ENST00000651865.1:c.172A>T	ENSP00000498567.1:p.Lys58Ter
ENST00000651913.1:c.122A>T
ENST00000652051.1:c.172A>T	ENSP00000498898.1:p.Lys58Ter
ENST00000652411.1:n.329A>T
ENST00000652501.1:c.172A>T	ENSP00000498261.1:p.Lys58Ter
ENST00000652541.1:c.172A>T	ENSP00000499206.1:p.Lys58Ter
ENST00000652727.1:c.172A>T	ENSP00000498650.1:p.Lys58Ter
ENST00000341484.11:c.-12A>T	ENSP00000345456.7:n.-12A>T
ENST00000420015.6:c.158+14A>T	ENSP00000410525.2:n.158+14A>T
ENST00000437198.6:c.172A>T	ENSP00000387911.2:p.Lys58Ter
ENST00000538472.5:c.172A>T	ENSP00000445659.1:p.Lys58Ter
ENST00000539279.5:c.172A>T	ENSP00000444381.1:p.Lys58Ter
ENST00000562896.1:c.244A>T	ENSP00000456982.1:p.Lys82Ter
ENST00000563641.5:c.172A>T	ENSP00000458103.1:p.Lys58Ter
ENST00000566021.1:n.298A>T
NM_001134477.2:c.-12A>T	NP_001127949.1:n.-12A>T
NM_001242992.1:c.158+14A>T	NP_001229921.1:n.158+14A>T
NM_002582.3:c.172A>T	NP_002573.1:p.Lys58Ter
XM_011522510.1:c.172A>T	XP_011520812.1:p.Lys58Ter
XM_011522511.1:c.172A>T	XP_011520813.1:p.Lys58Ter
XM_011522512.1:c.172A>T	XP_011520814.1:p.Lys58Ter
XM_011522513.1:c.-12A>T	XP_011520815.1:n.-12A>T
XM_011522514.1:c.172A>T	XP_011520816.1:p.Lys58Ter
NM_002582.4:c.172A>T MANE Select	NP_002573.1:p.Lys58Ter
XM_011522510.3:c.172A>T	XP_011520812.1:p.Lys58Ter
XM_011522511.2:c.172A>T	XP_011520813.1:p.Lys58Ter
XM_011522513.2:c.-12A>T	XP_011520815.1:n.-12A>T
XM_011522514.2:c.172A>T	XP_011520816.1:p.Lys58Ter
XM_017023258.2:c.172A>T	XP_016878747.1:p.Lys58Ter
XM_024450292.1:c.-1360A>T	XP_024306060.1:n.-1360A>T
XR_001751906.2:n.333A>T
XR_001751907.2:n.333A>T
NM_001134477.3:c.-12A>T	NP_001127949.1:n.-12A>T
NM_001242992.2:c.158+14A>T	NP_001229921.1:n.158+14A>T