Canonical Allele Identifier: CA278510978

Gene: PARN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.14584361T>C , CM000678.2:g.14584361T>C	GRCh38
NC_000016.9:g.14678218T>C , CM000678.1:g.14678218T>C	GRCh37
NC_000016.8:g.14585719T>C	NCBI36
NG_042871.1:g.50911A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_002582.4:c.1067A>G MANE Select	NP_002573.1:p.Asn356Ser
ENST00000437198.7:c.1067A>G MANE Select	ENSP00000387911.2:p.Asn356Ser
NM_001134477.2:c.884A>G	NP_001127949.1:p.Asn295Ser
NM_001134477.3:c.884A>G	NP_001127949.1:p.Asn295Ser
NM_001242992.1:c.929A>G	NP_001229921.1:p.Asn310Ser
NM_001242992.2:c.929A>G	NP_001229921.1:p.Asn310Ser
NM_002582.3:c.1067A>G	NP_002573.1:p.Asn356Ser
ENST00000341484.11:c.884A>G	ENSP00000345456.7:p.Asn295Ser
ENST00000420015.6:c.929A>G	ENSP00000410525.2:p.Asn310Ser
ENST00000437198.6:c.1067A>G	ENSP00000387911.2:p.Asn356Ser
ENST00000539279.5:c.542A>G	ENSP00000444381.1:p.Asn181Ser
ENST00000562715.1:n.105A>G
ENST00000563641.6:c.*831A>G	ENSP00000458103.1:n.*831A>G
ENST00000563697.5:n.74A>G
ENST00000564113.5:n.314A>G
ENST00000564113.6:n.1177A>G
ENST00000569444.5:c.532A>G
ENST00000650960.1:c.1067A>G	ENSP00000499110.1:p.Asn356Ser
ENST00000650990.1:c.1142A>G	ENSP00000498741.1:p.Asn381Ser
ENST00000651027.1:c.1067A>G	ENSP00000498640.1:p.Asn356Ser
ENST00000651049.1:c.1067A>G	ENSP00000498644.1:p.Asn356Ser
ENST00000651300.1:c.*961A>G	ENSP00000498294.1:n.*961A>G
ENST00000651348.1:c.*138A>G	ENSP00000498315.1:n.*138A>G
ENST00000651634.1:c.1067A>G	ENSP00000499078.1:p.Asn356Ser
ENST00000651760.1:c.2255A>G
ENST00000651865.1:c.992A>G	ENSP00000498567.1:p.Asn331Ser
ENST00000651913.1:c.1014A>G
ENST00000652051.1:c.1067A>G	ENSP00000498898.1:p.Asn356Ser
ENST00000652066.1:c.847A>G
ENST00000652411.1:n.1224A>G
ENST00000652501.1:c.1067A>G	ENSP00000498261.1:p.Asn356Ser
ENST00000652541.1:c.*801A>G	ENSP00000499206.1:n.*801A>G
ENST00000652727.1:c.980A>G	ENSP00000498650.1:p.Asn327Ser
ENST00000697471.1:n.1518A>G
ENST00000697472.1:n.1108A>G
ENST00000697473.1:n.2669A>G
ENST00000697474.1:c.1067A>G	ENSP00000513329.1:p.Asn356Ser
ENST00000697475.1:n.1222A>G
ENST00000697476.1:n.1200A>G
XM_011522510.1:c.1067A>G	XP_011520812.1:p.Asn356Ser
XM_011522510.3:c.1067A>G	XP_011520812.1:p.Asn356Ser
XM_011522511.1:c.1067A>G	XP_011520813.1:p.Asn356Ser
XM_011522511.2:c.1067A>G	XP_011520813.1:p.Asn356Ser
XM_011522512.1:c.1067A>G	XP_011520814.1:p.Asn356Ser
XM_011522513.1:c.884A>G	XP_011520815.1:p.Asn295Ser
XM_011522513.2:c.884A>G	XP_011520815.1:p.Asn295Ser
XM_011522514.1:c.1067A>G	XP_011520816.1:p.Asn356Ser
XM_011522514.2:c.1067A>G	XP_011520816.1:p.Asn356Ser
XM_017023258.2:c.989A>G	XP_016878747.1:p.Asn330Ser
XM_017023259.2:c.230A>G	XP_016878748.1:p.Asn77Ser
XM_017023260.1:c.230A>G	XP_016878749.1:p.Asn77Ser
XM_024450292.1:c.230A>G	XP_024306060.1:p.Asn77Ser
XR_001751906.2:n.1184A>G
XR_001751907.2:n.1184A>G