Canonical Allele Identifier: CA1425760901
Gene: PARL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.183867912G= , CM000665.2:g.183867912G= GRCh38
NC_000003.11:g.183585700G= , CM000665.1:g.183585700G= GRCh37
NC_000003.10:g.185068394G= NCBI36
NG_046164.1:g.21994C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000317096.9:c.274C= MANE Select ENSP00000325421.5:p.Pro92=
ENST00000638817.1:c.274C= ENSP00000492596.1:p.Pro92=
ENST00000639100.1:c.-420C= ENSP00000491186.1:n.-420C=
ENST00000639401.1:c.274C= ENSP00000491227.1:p.Pro92=
ENST00000639900.1:c.274C= ENSP00000491109.1:p.Pro92=
ENST00000311101.9:c.274C= ENSP00000310676.5:p.Pro92=
ENST00000317096.8:c.274C= ENSP00000325421.4:p.Pro92=
ENST00000421484.5:c.274C= ENSP00000404421.1:p.Pro92=
ENST00000435888.5:c.274C= ENSP00000402137.1:p.Pro92=
ENST00000449306.1:c.155C=
ENST00000469056.1:n.196C=
NM_001037639.1:c.274C= NP_001032728.1:p.Pro92=
NM_018622.5:c.274C= NP_061092.3:p.Pro92=
XM_005247582.3:c.274C= XP_005247639.1:p.Pro92=
XM_005247584.3:c.274C= XP_005247641.1:p.Pro92=
XM_005247587.1:c.-356C= XP_005247644.1:n.-356C=
NM_001037639.2:c.274C= NP_001032728.1:p.Pro92=
NM_001324436.1:c.274C= NP_001311365.1:p.Pro92=
NM_001324437.1:c.274C= NP_001311366.1:p.Pro92=
NM_001324438.1:c.274C= NP_001311367.1:p.Pro92=
NM_018622.6:c.274C= NP_061092.3:p.Pro92=
NR_136893.1:n.336C=
XM_005247582.5:c.274C= XP_005247639.1:p.Pro92=
XM_017006800.2:c.274C= XP_016862289.1:p.Pro92=
XM_017006801.1:c.274C= XP_016862290.1:p.Pro92=
XM_017006802.1:c.274C= XP_016862291.1:p.Pro92=
XM_017006803.1:c.-356C= XP_016862292.1:n.-356C=
XM_024453628.1:c.-300C= XP_024309396.1:n.-300C=
XM_024453629.1:c.-356C= XP_024309397.1:n.-356C=
XM_024453630.1:c.-420C= XP_024309398.1:n.-420C=
XM_024453631.1:c.-476C= XP_024309399.1:n.-476C=
XM_024453632.1:c.-476C= XP_024309400.1:n.-476C=
XM_024453633.1:c.-420C= XP_024309401.1:n.-420C=
NM_001037639.3:c.274C= NP_001032728.1:p.Pro92=
NM_001324436.2:c.274C= NP_001311365.1:p.Pro92=
NM_001324437.2:c.274C= NP_001311366.1:p.Pro92=
NM_001324438.2:c.274C= NP_001311367.1:p.Pro92=
NM_018622.7:c.274C= MANE Select NP_061092.3:p.Pro92=
NR_136893.2:n.308C=