Canonical Allele Identifier: CA15284311

Gene: PPM1L

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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