Canonical Allele Identifier: CA400769693

Gene: PPM1E TRIM37

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58982923T>A , CM000679.2:g.58982923T>A	GRCh38
NC_000017.10:g.57060284T>A , CM000679.1:g.57060284T>A	GRCh37
NC_000017.9:g.54415066T>A	NCBI36
NG_009298.1:g.128983A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_014906.5:c.*1892T>A (PPM1E) MANE Select	NP_055721.3:n.*1892T>A
ENST00000308249.4:c.*1892T>A (PPM1E) MANE Select	ENSP00000312411.2:n.*1892T>A
NM_001005207.2:c.2892-2A>T (TRIM37)	NP_001005207.1:n.2892-2A>T
NM_001005207.4:c.2892-2A>T (TRIM37)	NP_001005207.1:n.2892-2A>T
NM_001005207.5:c.2892-2A>T (TRIM37)	NP_001005207.1:n.2892-2A>T
NM_001320989.2:c.2775-2A>T (TRIM37)	NP_001307918.1:n.2775-2A>T
NM_001320989.3:c.2775-2A>T (TRIM37)	NP_001307918.1:n.2775-2A>T
NM_014906.4:c.*1892T>A (PPM1E)	NP_055721.3:n.*1892T>A
NR_048561.1:n.4089T>A (PPM1E)
ENST00000308249.3:c.*1892T>A (PPM1E)	ENSP00000312411.2:n.*1892T>A
ENST00000393066.7:c.2892-2A>T (TRIM37)	ENSP00000376785.3:n.2892-2A>T
ENST00000583945.5:c.160-2A>T (TRIM37)
ENST00000585287.5:c.351-2A>T (TRIM37)	ENSP00000464666.1:n.351-2A>T
XM_005257385.1:c.2919-2A>T (TRIM37)	XP_005257442.1:n.2919-2A>T
XM_005257390.1:c.2775-2A>T (TRIM37)	XP_005257447.1:n.2775-2A>T
XM_017024359.1:c.*1892T>A (PPM1E)	XP_016879848.1:n.*1892T>A
XM_017024662.1:c.2919-12824A>T (TRIM37)	XP_016880151.1:n.2919-12824A>T
XM_017024663.2:c.2892-12824A>T (TRIM37)	XP_016880152.1:n.2892-12824A>T
XM_017024667.1:c.2841-2A>T (TRIM37)	XP_016880156.1:n.2841-2A>T
XM_024450657.1:c.*1892T>A (PPM1E)	XP_024306425.1:n.*1892T>A