Canonical Allele Identifier: CA1415441211
Gene: PPM1L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.161059176C>G , CM000665.2:g.161059176C>G GRCh38
NC_000003.11:g.160776964C>G , CM000665.1:g.160776964C>G GRCh37
NC_000003.10:g.162259658C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000498165.6:c.575-6227C>G MANE Select ENSP00000417659.1:n.575-6227C>G
ENST00000295839.9:c.194-6227C>G ENSP00000295839.9:n.194-6227C>G
ENST00000464260.5:c.38-6227C>G ENSP00000420746.1:n.38-6227C>G
ENST00000480117.1:n.595-6227C>G
ENST00000498165.5:c.575-6227C>G ENSP00000417659.1:n.575-6227C>G
NM_139245.2:c.575-6227C>G NP_640338.2:n.575-6227C>G
XM_011512441.1:c.38-6227C>G XP_011510743.1:n.38-6227C>G
NM_001317911.1:c.194-6227C>G NP_001304840.1:n.194-6227C>G
NM_001317912.1:c.38-6227C>G NP_001304841.1:n.38-6227C>G
NM_139245.3:c.575-6227C>G NP_640338.2:n.575-6227C>G
NR_134243.1:n.595-6227C>G
NM_139245.4:c.575-6227C>G MANE Select NP_640338.2:n.575-6227C>G
NM_001317911.2:c.194-6227C>G NP_001304840.1:n.194-6227C>G
NM_001317912.2:c.38-6227C>G NP_001304841.1:n.38-6227C>G
NR_134243.2:n.595-6227C>G