Canonical Allele Identifier: CA2581494609
Gene: MEF2C HGNC NCBI
MEF2C-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs17560407
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.88887834A>T , CM000667.2:g.88887834A>T GRCh38
NC_000005.9:g.88183651A>T , CM000667.1:g.88183651A>T GRCh37
NC_000005.8:g.88219407A>T NCBI36
NG_023427.1:g.21272T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000636349.1:n.67-236T>A (MEF2C)
ENST00000637167.1:n.87-236T>A (MEF2C)
ENST00000637231.1:n.45-236T>A (MEF2C)
ENST00000637663.1:n.250-236T>A (MEF2C)
ENST00000340208.9:c.-239-236T>A (MEF2C) ENSP00000340874.5:n.-239-236T>A
ENST00000424173.6:c.-239-236T>A (MEF2C) ENSP00000389610.2:n.-239-236T>A
ENST00000503955.1:n.138-236T>A (MEF2C)
ENST00000515093.1:n.275-236T>A (MEF2C)
ENST00000625674.2:c.-236-236T>A (MEF2C) ENSP00000487430.1:n.-236-236T>A
ENST00000627659.2:c.-236-236T>A (MEF2C) ENSP00000486490.1:n.-236-236T>A
ENST00000629612.2:c.-236-236T>A (MEF2C) ENSP00000486554.1:n.-236-236T>A
NM_001131005.2:c.-239-236T>A (MEF2C) NP_001124477.1:n.-239-236T>A
NM_001193347.1:c.-239-236T>A (MEF2C) NP_001180276.1:n.-239-236T>A
NR_109941.1:n.156+4349A>T (MEF2C-AS1)
XM_006714618.1:c.-236-236T>A (MEF2C) XP_006714681.1:n.-236-236T>A
XM_006714619.1:c.-236-236T>A (MEF2C) XP_006714682.1:n.-236-236T>A
NM_001364329.1:c.-236-236T>A (MEF2C) NP_001351258.1:n.-236-236T>A
NM_001364330.1:c.-239-236T>A (MEF2C) NP_001351259.1:n.-239-236T>A
NM_001364334.1:c.-236-236T>A (MEF2C) NP_001351263.1:n.-236-236T>A
NR_136218.1:n.156+4349A>T (MEF2C-AS1)
NR_136219.1:n.156+4349A>T (MEF2C-AS1)
XM_011543396.3:c.-239-236T>A (MEF2C) XP_011541698.1:n.-239-236T>A
NM_001364329.2:c.-236-236T>A (MEF2C) NP_001351258.1:n.-236-236T>A
NM_001364330.2:c.-239-236T>A (MEF2C) NP_001351259.1:n.-239-236T>A
NM_001364334.2:c.-236-236T>A (MEF2C) NP_001351263.1:n.-236-236T>A
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