Canonical Allele Identifier: CA683656740

Gene: MAPKAPK5

Linked Data

• dbSNP Id: rs1382063473
• gnomAD v3: 12-111881298-T-A
• gnomAD v4: 12-111881298-T-A
• MyVariant Identifiers: chr12:g.112319102T>A (hg19) ; chr12:g.111881298T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.111881298T>A , CM000674.2:g.111881298T>A	GRCh38
NC_000012.11:g.112319102T>A , CM000674.1:g.112319102T>A	GRCh37
NC_000012.10:g.110803485T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000551404.7:c.660+771T>A	ENSP00000449381.2:n.660+771T>A
ENST00000550735.7:c.660+771T>A MANE Select	ENSP00000449667.2:n.660+771T>A
ENST00000549875.1:c.213+771T>A	ENSP00000473467.1:n.213+771T>A
ENST00000550735.6:c.660+771T>A	ENSP00000449667.2:n.660+771T>A
ENST00000551404.6:c.660+771T>A	ENSP00000449381.2:n.660+771T>A
ENST00000553053.5:c.213+771T>A	ENSP00000448408.2:n.213+771T>A
NM_003668.3:c.660+771T>A	NP_003659.2:n.660+771T>A
NM_139078.2:c.660+771T>A	NP_620777.1:n.660+771T>A
XM_005253979.2:c.-104+771T>A	XP_005254036.2:n.-104+771T>A
XM_011538909.1:c.660+771T>A	XP_011537211.1:n.660+771T>A
XM_011538910.1:c.660+771T>A	XP_011537212.1:n.660+771T>A
XM_011538911.1:c.660+771T>A	XP_011537213.1:n.660+771T>A
XM_011538912.1:c.660+771T>A	XP_011537214.1:n.660+771T>A
XM_011538913.1:c.660+771T>A	XP_011537215.1:n.660+771T>A
XM_011538914.1:c.660+771T>A	XP_011537216.1:n.660+771T>A
XM_011538915.1:c.660+771T>A	XP_011537217.1:n.660+771T>A
XM_011538916.1:c.660+771T>A	XP_011537218.1:n.660+771T>A
XM_011538917.1:c.570+771T>A	XP_011537219.1:n.570+771T>A
XM_011538918.1:c.453+771T>A	XP_011537220.1:n.453+771T>A
XM_011538919.1:c.381+771T>A	XP_011537221.1:n.381+771T>A
XM_011538920.1:c.120+771T>A	XP_011537222.1:n.120+771T>A
XM_011538921.1:c.120+771T>A	XP_011537223.1:n.120+771T>A
XM_011538922.1:c.120+771T>A	XP_011537224.1:n.120+771T>A
XR_944806.1:n.993+771T>A
XR_944807.1:n.993+771T>A
XM_017020125.1:c.462+771T>A	XP_016875614.1:n.462+771T>A
XM_017020126.1:c.453+771T>A	XP_016875615.1:n.453+771T>A
XM_017020127.1:c.381+771T>A	XP_016875616.1:n.381+771T>A
XM_017020128.1:c.381+771T>A	XP_016875617.1:n.381+771T>A
XM_017020129.1:c.381+771T>A	XP_016875618.1:n.381+771T>A
XM_017020130.1:c.381+771T>A	XP_016875619.1:n.381+771T>A
XM_017020131.1:c.381+771T>A	XP_016875620.1:n.381+771T>A
XM_017020132.1:c.120+771T>A	XP_016875621.1:n.120+771T>A
XM_017020133.1:c.120+771T>A	XP_016875622.1:n.120+771T>A
XM_017020134.1:c.120+771T>A	XP_016875623.1:n.120+771T>A
XM_017020135.2:c.120+771T>A	XP_016875624.1:n.120+771T>A
XM_017020136.1:c.120+771T>A	XP_016875625.1:n.120+771T>A
XM_017020137.2:c.120+771T>A	XP_016875626.1:n.120+771T>A
XM_017020138.1:c.-104+771T>A	XP_016875627.1:n.-104+771T>A
XM_017020139.1:c.-104+771T>A	XP_016875628.1:n.-104+771T>A
XM_024449247.1:c.120+771T>A	XP_024305015.1:n.120+771T>A
NM_001371479.1:c.660+771T>A	NP_001358408.1:n.660+771T>A
NM_001371480.1:c.660+771T>A	NP_001358409.1:n.660+771T>A
NM_001371481.1:c.580-2283T>A	NP_001358410.1:n.580-2283T>A
NM_001371482.1:c.570+771T>A	NP_001358411.1:n.570+771T>A
NM_001371483.1:c.570+771T>A	NP_001358412.1:n.570+771T>A
NM_001371484.1:c.558+771T>A	NP_001358413.1:n.558+771T>A
NM_001371485.1:c.453+771T>A	NP_001358414.1:n.453+771T>A
NM_001371486.1:c.453+771T>A	NP_001358415.1:n.453+771T>A
NM_001371487.1:c.363+771T>A	NP_001358416.1:n.363+771T>A
NM_003668.4:c.660+771T>A MANE Select	NP_003659.2:n.660+771T>A
NM_139078.3:c.660+771T>A	NP_620777.1:n.660+771T>A