Canonical Allele Identifier: CA243682472
Community Standard Title: NM_003668.4(MAPKAPK5):c.590C>T (p.Ala197Val)
Gene: MAPKAPK5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111880457C>T , CM000674.2:g.111880457C>T GRCh38
NC_000012.11:g.112318261C>T , CM000674.1:g.112318261C>T GRCh37
NC_000012.10:g.110802644C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_003668.4:c.590C>T MANE Select NP_003659.2:p.Ala197Val
ENST00000550735.7:c.590C>T MANE Select ENSP00000449667.2:p.Ala197Val
NM_001371479.1:c.590C>T NP_001358408.1:p.Ala197Val
NM_001371480.1:c.590C>T NP_001358409.1:p.Ala197Val
NM_001371481.1:c.580-3124C>T NP_001358410.1:n.580-3124C>T
NM_001371482.1:c.500C>T NP_001358411.1:p.Ala167Val
NM_001371483.1:c.500C>T NP_001358412.1:p.Ala167Val
NM_001371484.1:c.488C>T NP_001358413.1:p.Ala163Val
NM_001371485.1:c.383C>T NP_001358414.1:p.Ala128Val
NM_001371486.1:c.383C>T NP_001358415.1:p.Ala128Val
NM_001371487.1:c.293C>T NP_001358416.1:p.Ala98Val
NM_003668.3:c.590C>T NP_003659.2:p.Ala197Val
NM_139078.2:c.590C>T NP_620777.1:p.Ala197Val
NM_139078.3:c.590C>T NP_620777.1:p.Ala197Val
ENST00000549875.1:c.143C>T ENSP00000473467.1:p.Ala48Val
ENST00000550735.6:c.590C>T ENSP00000449667.2:p.Ala197Val
ENST00000551404.6:c.590C>T ENSP00000449381.2:p.Ala197Val
ENST00000551404.7:c.590C>T ENSP00000449381.2:p.Ala197Val
ENST00000553053.5:c.143C>T ENSP00000448408.2:p.Ala48Val
XM_005253979.2:c.-174C>T XP_005254036.2:n.-174C>T
XM_011538909.1:c.590C>T XP_011537211.1:p.Ala197Val
XM_011538910.1:c.590C>T XP_011537212.1:p.Ala197Val
XM_011538911.1:c.590C>T XP_011537213.1:p.Ala197Val
XM_011538912.1:c.590C>T XP_011537214.1:p.Ala197Val
XM_011538913.1:c.590C>T XP_011537215.1:p.Ala197Val
XM_011538914.1:c.590C>T XP_011537216.1:p.Ala197Val
XM_011538915.1:c.590C>T XP_011537217.1:p.Ala197Val
XM_011538916.1:c.590C>T XP_011537218.1:p.Ala197Val
XM_011538917.1:c.500C>T XP_011537219.1:p.Ala167Val
XM_011538918.1:c.383C>T XP_011537220.1:p.Ala128Val
XM_011538919.1:c.311C>T XP_011537221.1:p.Ala104Val
XM_011538920.1:c.50C>T XP_011537222.1:p.Ala17Val
XM_011538921.1:c.50C>T XP_011537223.1:p.Ala17Val
XM_011538922.1:c.50C>T XP_011537224.1:p.Ala17Val
XM_017020125.1:c.392C>T XP_016875614.1:p.Ala131Val
XM_017020126.1:c.383C>T XP_016875615.1:p.Ala128Val
XM_017020127.1:c.311C>T XP_016875616.1:p.Ala104Val
XM_017020128.1:c.311C>T XP_016875617.1:p.Ala104Val
XM_017020129.1:c.311C>T XP_016875618.1:p.Ala104Val
XM_017020130.1:c.311C>T XP_016875619.1:p.Ala104Val
XM_017020131.1:c.311C>T XP_016875620.1:p.Ala104Val
XM_017020132.1:c.50C>T XP_016875621.1:p.Ala17Val
XM_017020133.1:c.50C>T XP_016875622.1:p.Ala17Val
XM_017020134.1:c.50C>T XP_016875623.1:p.Ala17Val
XM_017020135.2:c.50C>T XP_016875624.1:p.Ala17Val
XM_017020136.1:c.50C>T XP_016875625.1:p.Ala17Val
XM_017020137.2:c.50C>T XP_016875626.1:p.Ala17Val
XM_017020138.1:c.-174C>T XP_016875627.1:n.-174C>T
XM_017020139.1:c.-174C>T XP_016875628.1:n.-174C>T
XM_024449247.1:c.50C>T XP_024305015.1:p.Ala17Val
XR_944806.1:n.923C>T
XR_944807.1:n.923C>T