Canonical Allele Identifier: CA1425760895
Gene: PARL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.183867903T= , CM000665.2:g.183867903T= GRCh38
NC_000003.11:g.183585691T= , CM000665.1:g.183585691T= GRCh37
NC_000003.10:g.185068385T= NCBI36
NG_046164.1:g.22003A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000317096.9:c.283A= MANE Select ENSP00000325421.5:p.Ile95=
ENST00000638817.1:c.283A= ENSP00000492596.1:p.Ile95=
ENST00000639100.1:c.-411A= ENSP00000491186.1:n.-411A=
ENST00000639401.1:c.283A= ENSP00000491227.1:p.Ile95=
ENST00000639900.1:c.283A= ENSP00000491109.1:p.Ile95=
ENST00000311101.9:c.283A= ENSP00000310676.5:p.Ile95=
ENST00000317096.8:c.283A= ENSP00000325421.4:p.Ile95=
ENST00000421484.5:c.283A= ENSP00000404421.1:p.Ile95=
ENST00000435888.5:c.283A= ENSP00000402137.1:p.Ile95=
ENST00000449306.1:c.164A=
ENST00000469056.1:n.205A=
NM_001037639.1:c.283A= NP_001032728.1:p.Ile95=
NM_018622.5:c.283A= NP_061092.3:p.Ile95=
XM_005247582.3:c.283A= XP_005247639.1:p.Ile95=
XM_005247584.3:c.283A= XP_005247641.1:p.Ile95=
XM_005247587.1:c.-347A= XP_005247644.1:n.-347A=
NM_001037639.2:c.283A= NP_001032728.1:p.Ile95=
NM_001324436.1:c.283A= NP_001311365.1:p.Ile95=
NM_001324437.1:c.283A= NP_001311366.1:p.Ile95=
NM_001324438.1:c.283A= NP_001311367.1:p.Ile95=
NM_018622.6:c.283A= NP_061092.3:p.Ile95=
NR_136893.1:n.345A=
XM_005247582.5:c.283A= XP_005247639.1:p.Ile95=
XM_017006800.2:c.283A= XP_016862289.1:p.Ile95=
XM_017006801.1:c.283A= XP_016862290.1:p.Ile95=
XM_017006802.1:c.283A= XP_016862291.1:p.Ile95=
XM_017006803.1:c.-347A= XP_016862292.1:n.-347A=
XM_024453628.1:c.-291A= XP_024309396.1:n.-291A=
XM_024453629.1:c.-347A= XP_024309397.1:n.-347A=
XM_024453630.1:c.-411A= XP_024309398.1:n.-411A=
XM_024453631.1:c.-467A= XP_024309399.1:n.-467A=
XM_024453632.1:c.-467A= XP_024309400.1:n.-467A=
XM_024453633.1:c.-411A= XP_024309401.1:n.-411A=
NM_001037639.3:c.283A= NP_001032728.1:p.Ile95=
NM_001324436.2:c.283A= NP_001311365.1:p.Ile95=
NM_001324437.2:c.283A= NP_001311366.1:p.Ile95=
NM_001324438.2:c.283A= NP_001311367.1:p.Ile95=
NM_018622.7:c.283A= MANE Select NP_061092.3:p.Ile95=
NR_136893.2:n.317A=