Canonical Allele Identifier: CA15244541
Gene: PARL HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1402000

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.183867753T>C , CM000665.2:g.183867753T>C GRCh38
NC_000003.11:g.183585541T>C , CM000665.1:g.183585541T>C GRCh37
NC_000003.10:g.185068235T>C NCBI36
NG_046164.1:g.22153A>G

Transcript Alleles

HGVS Amino-acid change
NM_001037639.1:c.321+112A>G VV NP_001032728.1:p.=
NM_018622.5:c.321+112A>G VV NP_061092.3:p.=
XM_005247582.3:c.321+112A>G XP_005247639.1:p.=
XM_005247584.3:c.321+112A>G XP_005247641.1:p.=
XM_005247587.1:c.-309+112A>G XP_005247644.1:p.=
NM_001037639.2:c.321+112A>G VV NP_001032728.1:p.=
NM_001324436.1:c.321+112A>G VV NP_001311365.1:p.=
NM_001324437.1:c.321+112A>G VV NP_001311366.1:p.=
NM_001324438.1:c.321+112A>G VV NP_001311367.1:p.=
NM_018622.6:c.321+112A>G VV NP_061092.3:p.=
NR_136893.1:n.383+112A>G
XM_005247582.5:c.321+112A>G XP_005247639.1:p.=
XM_017006800.2:c.321+112A>G XP_016862289.1:p.=
XM_017006801.1:c.321+112A>G XP_016862290.1:p.=
XM_017006802.1:c.321+112A>G XP_016862291.1:p.=
XM_017006803.1:c.-309+112A>G XP_016862292.1:p.=
XM_024453628.1:c.-253+112A>G XP_024309396.1:p.=
XM_024453629.1:c.-309+112A>G XP_024309397.1:p.=
XM_024453630.1:c.-373+112A>G XP_024309398.1:p.=
XM_024453631.1:c.-429+112A>G XP_024309399.1:p.=
XM_024453632.1:c.-429+112A>G XP_024309400.1:p.=
XM_024453633.1:c.-373+112A>G XP_024309401.1:p.=
ENST00000311101.9:c.321+112A>G ENSP00000310676.5:p.=
ENST00000317096.8:c.321+112A>G ENSP00000325421.4:p.=
ENST00000421484.5:c.321+112A>G ENSP00000404421.1:p.=
ENST00000435888.5:c.321+112A>G ENSP00000402137.1:p.=
ENST00000449306.1:n.202+112A>G
ENST00000469056.1:n.243+112A>G