Canonical Allele Identifier: CA14006244

Gene: PPM1A

Linked Data

• dbSNP Id: rs7154773
• gnomAD v2: 14-60749118-G-C
• gnomAD v3: 14-60282400-G-C
• gnomAD v4: 14-60282400-G-C
• MyVariant Identifiers: chr14:g.60749118G>C (hg19) ; chr14:g.60282400G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.60282400G>C , CM000676.2:g.60282400G>C	GRCh38
NC_000014.8:g.60749118G>C , CM000676.1:g.60749118G>C	GRCh37
NC_000014.7:g.59818871G>C	NCBI36
NG_029698.1:g.41649G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000395076.9:c.-20-284G>C MANE Select	ENSP00000378514.4:n.-20-284G>C
ENST00000325642.7:c.200-284G>C	ENSP00000327255.3:n.200-284G>C
ENST00000325658.3:c.-20-284G>C	ENSP00000314850.3:n.-20-284G>C
ENST00000395076.8:c.-20-284G>C	ENSP00000378514.4:n.-20-284G>C
ENST00000525399.2:c.-20-284G>C	ENSP00000435398.2:n.-20-284G>C
ENST00000528241.2:c.-20-284G>C	ENSP00000431453.2:n.-20-284G>C
ENST00000531143.6:c.*5-284G>C	ENSP00000437200.2:n.*5-284G>C
ENST00000531937.1:c.-20-284G>C	ENSP00000435575.1:n.-20-284G>C
ENST00000532036.2:c.200-284G>C	ENSP00000436445.2:n.200-284G>C
NM_021003.4:c.-20-284G>C	NP_066283.1:n.-20-284G>C
NM_177951.2:c.-20-284G>C	NP_808820.1:n.-20-284G>C
NM_177952.2:c.200-284G>C	NP_808821.2:n.200-284G>C
XM_005267779.1:c.-20-284G>C	XP_005267836.1:n.-20-284G>C
XM_005267781.1:c.-20-284G>C	XP_005267838.1:n.-20-284G>C
XM_006720179.1:c.-20-284G>C	XP_006720242.1:n.-20-284G>C
XM_011536857.1:c.212-284G>C	XP_011535159.1:n.212-284G>C
XM_011536858.1:c.212-284G>C	XP_011535160.1:n.212-284G>C
XM_011536859.1:c.212-284G>C	XP_011535161.1:n.212-284G>C
XM_011536860.1:c.212-284G>C	XP_011535162.1:n.212-284G>C
XM_011536861.1:c.212-284G>C	XP_011535163.1:n.212-284G>C
XM_011536862.1:c.212-284G>C	XP_011535164.1:n.212-284G>C
XM_011536863.1:c.212-284G>C	XP_011535165.1:n.212-284G>C
XM_011536864.1:c.212-284G>C	XP_011535166.1:n.212-284G>C
XM_011536865.1:c.212-284G>C	XP_011535167.1:n.212-284G>C
XM_011536866.1:c.143-284G>C	XP_011535168.1:n.143-284G>C
XM_011536867.1:c.143-284G>C	XP_011535169.1:n.143-284G>C
XM_011536868.1:c.143-284G>C	XP_011535170.1:n.143-284G>C
XM_011536869.1:c.143-284G>C	XP_011535171.1:n.143-284G>C
XM_011536870.1:c.143-284G>C	XP_011535172.1:n.143-284G>C
XM_011536871.1:c.143-284G>C	XP_011535173.1:n.143-284G>C
XM_011536872.1:c.143-284G>C	XP_011535174.1:n.143-284G>C
XM_011536873.1:c.143-284G>C	XP_011535175.1:n.143-284G>C
XM_011536874.1:c.143-284G>C	XP_011535176.1:n.143-284G>C
XM_011536875.1:c.143-284G>C	XP_011535177.1:n.143-284G>C
XM_011536876.1:c.143-284G>C	XP_011535178.1:n.143-284G>C
XM_011536877.1:c.143-284G>C	XP_011535179.1:n.143-284G>C
XM_011536878.1:c.-20-284G>C	XP_011535180.1:n.-20-284G>C
XM_011536879.1:c.-20-284G>C	XP_011535181.1:n.-20-284G>C
XM_011536880.1:c.-20-284G>C	XP_011535182.1:n.-20-284G>C
XM_011536881.1:c.-20-284G>C	XP_011535183.1:n.-20-284G>C
XM_011536882.1:c.-20-284G>C	XP_011535184.1:n.-20-284G>C
XM_011536883.1:c.-20-284G>C	XP_011535185.1:n.-20-284G>C
XM_011536884.1:c.-20-284G>C	XP_011535186.1:n.-20-284G>C
XM_011536879.3:c.-20-284G>C	XP_011535181.1:n.-20-284G>C
XM_011536880.3:c.-20-284G>C	XP_011535182.1:n.-20-284G>C
XM_011536881.3:c.-20-284G>C	XP_011535183.1:n.-20-284G>C
XM_011536882.2:c.-20-284G>C	XP_011535184.1:n.-20-284G>C
XM_017021381.1:c.212-284G>C	XP_016876870.1:n.212-284G>C
XM_017021382.1:c.143-284G>C	XP_016876871.1:n.143-284G>C
XM_017021383.1:c.59-284G>C	XP_016876872.1:n.59-284G>C
XM_017021384.1:c.-20-284G>C	XP_016876873.1:n.-20-284G>C
XM_017021385.1:c.-20-284G>C	XP_016876874.1:n.-20-284G>C
XM_017021386.1:c.-20-284G>C	XP_016876875.1:n.-20-284G>C
XM_017021387.1:c.-20-284G>C	XP_016876876.1:n.-20-284G>C
XM_024449637.1:c.-20-284G>C	XP_024305405.1:n.-20-284G>C
NM_021003.5:c.-20-284G>C MANE Select	NP_066283.1:n.-20-284G>C
NM_177951.3:c.-20-284G>C	NP_808820.1:n.-20-284G>C
NM_177952.3:c.200-284G>C	NP_808821.2:n.200-284G>C