Canonical Allele Identifier: CA395184629

Gene: PARN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.14447082C>A , CM000678.2:g.14447082C>A	GRCh38
NC_000016.9:g.14540939C>A , CM000678.1:g.14540939C>A	GRCh37
NC_000016.8:g.14448440C>A	NCBI36
NG_042871.1:g.188190G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_002582.4:c.1671-1G>T MANE Select	NP_002573.1:n.1671-1G>T
ENST00000437198.7:c.1671-1G>T MANE Select	ENSP00000387911.2:n.1671-1G>T
NM_001134477.2:c.1488-1G>T	NP_001127949.1:n.1488-1G>T
NM_001134477.3:c.1488-1G>T	NP_001127949.1:n.1488-1G>T
NM_001242992.1:c.1533-1G>T	NP_001229921.1:n.1533-1G>T
NM_001242992.2:c.1533-1G>T	NP_001229921.1:n.1533-1G>T
NM_002582.3:c.1671-1G>T	NP_002573.1:n.1671-1G>T
ENST00000341484.11:c.1488-1G>T	ENSP00000345456.7:n.1488-1G>T
ENST00000420015.6:c.1533-1G>T	ENSP00000410525.2:n.1533-1G>T
ENST00000437198.6:c.1671-1G>T	ENSP00000387911.2:n.1671-1G>T
ENST00000539279.5:c.1146-1G>T	ENSP00000444381.1:n.1146-1G>T
ENST00000564882.5:n.328-1G>T
ENST00000650990.1:c.1746-1G>T	ENSP00000498741.1:n.1746-1G>T
ENST00000651300.1:c.*1478-1G>T	ENSP00000498294.1:n.*1478-1G>T
ENST00000651348.1:c.*742-1G>T	ENSP00000498315.1:n.*742-1G>T
ENST00000651760.1:c.2859-1G>T
ENST00000651865.1:c.1596-1G>T	ENSP00000498567.1:n.1596-1G>T
ENST00000652051.1:c.*447-1G>T	ENSP00000498898.1:n.*447-1G>T
ENST00000652066.1:c.1572-1G>T
ENST00000652541.1:c.*1503-1G>T	ENSP00000499206.1:n.*1503-1G>T
ENST00000652727.1:c.1497-1G>T	ENSP00000498650.1:n.1497-1G>T
ENST00000697471.1:n.2122-1G>T
ENST00000697472.1:n.1712-1G>T
ENST00000697473.1:n.3273-1G>T
ENST00000697474.1:c.1671-1G>T	ENSP00000513329.1:n.1671-1G>T