Canonical Allele Identifier: CA394817963

Gene: PARN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.14629595A>G , CM000678.2:g.14629595A>G	GRCh38
NC_000016.9:g.14723452A>G , CM000678.1:g.14723452A>G	GRCh37
NC_000016.8:g.14630953A>G	NCBI36
NG_042871.1:g.5677T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_002582.4:c.97+2T>C MANE Select	NP_002573.1:n.97+2T>C
ENST00000437198.7:c.97+2T>C MANE Select	ENSP00000387911.2:n.97+2T>C
NM_001134477.2:c.-87+2T>C	NP_001127949.1:n.-87+2T>C
NM_001134477.3:c.-87+2T>C	NP_001127949.1:n.-87+2T>C
NM_001242992.1:c.97+2T>C	NP_001229921.1:n.97+2T>C
NM_001242992.2:c.97+2T>C	NP_001229921.1:n.97+2T>C
NM_002582.3:c.97+2T>C	NP_002573.1:n.97+2T>C
ENST00000341484.11:c.-87+2T>C	ENSP00000345456.7:n.-87+2T>C
ENST00000420015.6:c.97+2T>C	ENSP00000410525.2:n.97+2T>C
ENST00000437198.6:c.97+2T>C	ENSP00000387911.2:n.97+2T>C
ENST00000538472.5:c.97+2T>C	ENSP00000445659.1:n.97+2T>C
ENST00000539279.5:c.97+2T>C	ENSP00000444381.1:n.97+2T>C
ENST00000562896.1:c.169+2T>C	ENSP00000456982.1:n.169+2T>C
ENST00000563641.5:c.97+2T>C	ENSP00000458103.1:n.97+2T>C
ENST00000563641.6:c.97+2T>C	ENSP00000458103.1:n.97+2T>C
ENST00000564113.6:n.207+2T>C
ENST00000566021.1:n.223+2T>C
ENST00000650960.1:c.97+2T>C	ENSP00000499110.1:n.97+2T>C
ENST00000650990.1:c.97+2T>C	ENSP00000498741.1:n.97+2T>C
ENST00000651027.1:c.97+2T>C	ENSP00000498640.1:n.97+2T>C
ENST00000651049.1:c.97+2T>C	ENSP00000498644.1:n.97+2T>C
ENST00000651241.1:n.207+2T>C
ENST00000651300.1:c.97+2T>C	ENSP00000498294.1:n.97+2T>C
ENST00000651348.1:c.97+2T>C	ENSP00000498315.1:n.97+2T>C
ENST00000651634.1:c.97+2T>C	ENSP00000499078.1:n.97+2T>C
ENST00000651865.1:c.97+2T>C	ENSP00000498567.1:n.97+2T>C
ENST00000651913.1:c.47+2T>C
ENST00000652051.1:c.97+2T>C	ENSP00000498898.1:n.97+2T>C
ENST00000652411.1:n.254+2T>C
ENST00000652501.1:c.97+2T>C	ENSP00000498261.1:n.97+2T>C
ENST00000652541.1:c.97+2T>C	ENSP00000499206.1:n.97+2T>C
ENST00000652727.1:c.97+2T>C	ENSP00000498650.1:n.97+2T>C
ENST00000697472.1:n.243+2T>C
ENST00000697473.1:n.222+2T>C
ENST00000697474.1:c.97+2T>C	ENSP00000513329.1:n.97+2T>C
ENST00000697475.1:n.252+2T>C
ENST00000697476.1:n.230+2T>C
ENST00000697477.1:n.232+2T>C
XM_011522510.1:c.97+2T>C	XP_011520812.1:n.97+2T>C
XM_011522510.3:c.97+2T>C	XP_011520812.1:n.97+2T>C
XM_011522511.1:c.97+2T>C	XP_011520813.1:n.97+2T>C
XM_011522511.2:c.97+2T>C	XP_011520813.1:n.97+2T>C
XM_011522512.1:c.97+2T>C	XP_011520814.1:n.97+2T>C
XM_011522513.1:c.-87+2T>C	XP_011520815.1:n.-87+2T>C
XM_011522513.2:c.-87+2T>C	XP_011520815.1:n.-87+2T>C
XM_011522514.1:c.97+2T>C	XP_011520816.1:n.97+2T>C
XM_011522514.2:c.97+2T>C	XP_011520816.1:n.97+2T>C
XM_017023258.2:c.97+2T>C	XP_016878747.1:n.97+2T>C
XM_024450292.1:c.-1435+2T>C	XP_024306060.1:n.-1435+2T>C
XR_001751906.2:n.258+2T>C
XR_001751907.2:n.258+2T>C