Canonical Allele Identifier: CA1364038345

Gene: MAPKAPK3

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50622900A= , CM000665.2:g.50622900A=	GRCh38
NC_000003.11:g.50660331A= , CM000665.1:g.50660331A=	GRCh37
NC_000003.10:g.50635335A=	NCBI36
NG_051548.1:g.16039A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621469.5:c.219+5116A= MANE Select	ENSP00000478922.1:n.219+5116A=
ENST00000357955.6:c.219+5116A=	ENSP00000350639.2:n.219+5116A=
ENST00000430409.5:c.219+5116A=	ENSP00000410970.1:n.219+5116A=
ENST00000446044.5:c.219+5116A=	ENSP00000396467.1:n.219+5116A=
ENST00000457064.1:c.219+5116A=	ENSP00000402045.1:n.219+5116A=
ENST00000621469.4:c.219+5116A=	ENSP00000478922.1:n.219+5116A=
NM_001243925.1:c.219+5116A=	NP_001230854.1:n.219+5116A=
NM_001243926.1:c.219+5116A=	NP_001230855.1:n.219+5116A=
NM_004635.4:c.219+5116A=	NP_004626.1:n.219+5116A=
XR_940501.1:n.341+5116A=
XR_940501.2:n.345+5116A=
NM_001243925.2:c.219+5116A= MANE Select	NP_001230854.1:n.219+5116A=
NM_001243926.2:c.219+5116A=	NP_001230855.1:n.219+5116A=
NM_004635.5:c.219+5116A=	NP_004626.1:n.219+5116A=