Canonical Allele Identifier: CA707378935

Gene: PPM1A

Linked Data

• dbSNP Id: rs1300172405
• gnomAD v3: 14-60289173-TG-T
• gnomAD v4: 14-60289173-TG-T
• MyVariant Identifiers: chr14:g.60755892del (hg19) ; chr14:g.60289174del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.60289174del , CM000676.2:g.60289174del	GRCh38
NC_000014.8:g.60755892del , CM000676.1:g.60755892del	GRCh37
NC_000014.7:g.59825645del	NCBI36
NG_029698.1:g.48423del

Transcript Alleles

HGVS	Amino-acid change
ENST00000395076.9:c.953-632del MANE Select	ENSP00000378514.4:n.953-632del
ENST00000325642.7:c.1172-632del	ENSP00000327255.3:n.1172-632del
ENST00000395076.8:c.953-632del	ENSP00000378514.4:n.953-632del
ENST00000531143.6:c.*977-632del	ENSP00000437200.2:n.*977-632del
ENST00000532036.2:c.429-632del	ENSP00000436445.2:n.429-632del
NM_021003.4:c.953-632del	NP_066283.1:n.953-632del
NM_177952.2:c.1172-632del	NP_808821.2:n.1172-632del
XM_005267779.1:c.953-632del	XP_005267836.1:n.953-632del
XM_005267781.1:c.953-632del	XP_005267838.1:n.953-632del
XM_006720179.1:c.953-632del	XP_006720242.1:n.953-632del
XM_011536857.1:c.1184-632del	XP_011535159.1:n.1184-632del
XM_011536858.1:c.1184-632del	XP_011535160.1:n.1184-632del
XM_011536859.1:c.1184-632del	XP_011535161.1:n.1184-632del
XM_011536860.1:c.1184-632del	XP_011535162.1:n.1184-632del
XM_011536861.1:c.1184-632del	XP_011535163.1:n.1184-632del
XM_011536862.1:c.1184-632del	XP_011535164.1:n.1184-632del
XM_011536863.1:c.1184-632del	XP_011535165.1:n.1184-632del
XM_011536864.1:c.1184-632del	XP_011535166.1:n.1184-632del
XM_011536865.1:c.1184-632del	XP_011535167.1:n.1184-632del
XM_011536866.1:c.1115-632del	XP_011535168.1:n.1115-632del
XM_011536867.1:c.1115-632del	XP_011535169.1:n.1115-632del
XM_011536868.1:c.1115-632del	XP_011535170.1:n.1115-632del
XM_011536869.1:c.1115-632del	XP_011535171.1:n.1115-632del
XM_011536870.1:c.1115-632del	XP_011535172.1:n.1115-632del
XM_011536871.1:c.1115-632del	XP_011535173.1:n.1115-632del
XM_011536872.1:c.1115-632del	XP_011535174.1:n.1115-632del
XM_011536873.1:c.1115-632del	XP_011535175.1:n.1115-632del
XM_011536874.1:c.1115-632del	XP_011535176.1:n.1115-632del
XM_011536875.1:c.1115-632del	XP_011535177.1:n.1115-632del
XM_011536876.1:c.1115-632del	XP_011535178.1:n.1115-632del
XM_011536877.1:c.1115-632del	XP_011535179.1:n.1115-632del
XM_011536878.1:c.953-632del	XP_011535180.1:n.953-632del
XM_011536879.1:c.953-632del	XP_011535181.1:n.953-632del
XM_011536880.1:c.953-632del	XP_011535182.1:n.953-632del
XM_011536881.1:c.953-632del	XP_011535183.1:n.953-632del
XM_011536882.1:c.953-632del	XP_011535184.1:n.953-632del
XM_011536883.1:c.953-632del	XP_011535185.1:n.953-632del
XM_011536884.1:c.953-632del	XP_011535186.1:n.953-632del
XM_011536879.3:c.953-632del	XP_011535181.1:n.953-632del
XM_011536880.3:c.953-632del	XP_011535182.1:n.953-632del
XM_011536881.3:c.953-632del	XP_011535183.1:n.953-632del
XM_011536882.2:c.953-632del	XP_011535184.1:n.953-632del
XM_017021381.1:c.1184-632del	XP_016876870.1:n.1184-632del
XM_017021382.1:c.1115-632del	XP_016876871.1:n.1115-632del
XM_017021383.1:c.1031-632del	XP_016876872.1:n.1031-632del
XM_017021384.1:c.953-632del	XP_016876873.1:n.953-632del
XM_017021385.1:c.953-632del	XP_016876874.1:n.953-632del
XM_017021386.1:c.953-632del	XP_016876875.1:n.953-632del
XM_017021387.1:c.953-632del	XP_016876876.1:n.953-632del
XM_024449637.1:c.953-632del	XP_024305405.1:n.953-632del
NM_021003.5:c.953-632del MANE Select	NP_066283.1:n.953-632del
NM_177952.3:c.1172-632del	NP_808821.2:n.1172-632del