Canonical Allele Identifier: CA2838275466

Gene: ZFPM2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.105424763T>A , CM000670.2:g.105424763T>A	GRCh38
NC_000008.10:g.106436991T>A , CM000670.1:g.106436991T>A	GRCh37
NC_000008.9:g.106506167T>A	NCBI36
NG_011723.1:g.110845T>A
NG_011723.2:g.110845T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407775.7:c.199+5461T>A MANE Select	ENSP00000384179.2:n.199+5461T>A
ENST00000407775.6:c.199+5461T>A	ENSP00000384179.2:n.199+5461T>A
ENST00000511341.6:n.939+5461T>A
ENST00000520027.5:c.-198+5461T>A	ENSP00000428149.1:n.-198+5461T>A
ENST00000520492.5:c.-198+5461T>A	ENSP00000430757.1:n.-198+5461T>A
ENST00000522160.1:n.159+5461T>A
ENST00000524235.5:n.412+5461T>A
NM_012082.3:c.199+5461T>A	NP_036214.2:n.199+5461T>A
XM_011516946.1:c.238+5461T>A	XP_011515248.1:n.238+5461T>A
XM_011516947.1:c.169+5461T>A	XP_011515249.1:n.169+5461T>A
XM_011516948.1:c.41-19517T>A	XP_011515250.1:n.41-19517T>A
XM_011516949.1:c.238+5461T>A	XP_011515251.1:n.238+5461T>A
NM_001362836.1:c.41-19517T>A	NP_001349765.1:n.41-19517T>A
NM_001362837.1:c.-198+5461T>A	NP_001349766.1:n.-198+5461T>A
XM_011516947.3:c.169+5461T>A	XP_011515249.1:n.169+5461T>A
NM_012082.4:c.199+5461T>A MANE Select	NP_036214.2:n.199+5461T>A
NM_001362836.2:c.41-19517T>A	NP_001349765.1:n.41-19517T>A
NM_001362837.2:c.-198+5461T>A	NP_001349766.1:n.-198+5461T>A